Substituted pyrazolo[1,5-A]pyrazine compounds as ret kinase inhibitors

ABSTRACT

Provided herein are compounds of the Formula I: 
                         
and stereoisomers and pharmaceutically acceptable salts or solvates thereof, in which A, B, D, E, X 1 , X 2 , X 3  and X 4  have the meanings given in the specification, which are inhibitors of RET kinase and are useful in the treatment and prevention of diseases which can be treated with a RET kinase inhibitor, including diseases or disorders mediated by a RET kinase.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a Continuation Application of U.S. application Ser. No. 16/478,071, filed Jul. 15, 2019, which is a National Stage Application filed under 35 U.S.C. § 371 of PCT/US2018/014279, filed Jan. 18, 2018, which claims priority to U.S. Provisional Application Ser. No. 62/447,862, filed on Jan. 18, 2017, each of which is hereby incorporated by reference in its entirety.

INCORPORATION BY REFERENCE

The content of the text file labeled “121US2SequenceListing.txt”, which was created on Jan. 10, 2022, and is 12 KB in size, is incorporated herein by reference in its entirety.

BACKGROUND

The present disclosure relates to novel compounds which exhibit Rearranged during Transfection (RET) kinase inhibition, pharmaceutical compositions comprising the compounds, processes for making the compounds, and the use of the compounds in therapy. More particularly, it relates to substituted pyrazolo[1,5-a]pyrazine compounds useful in the treatment and prevention of diseases which can be treated with a RET kinase inhibitor, including RET-associated diseases and disorders.

RET is a single-pass transmembrane receptor belonging to the tyrosine kinase superfamily that is required for normal development, maturation and maintenance of several tissues and cell types (Mulligan, L. M., Nature Reviews Cancer, 2014, 14, 173-186). The extracellular portion of the RET kinase contains four calcium-dependent cadherin-like repeats involved in ligand binding and a juxtamembrane cysteine-rich region necessary for the correct folding of the RET extracellular domain, while the cytoplasmic portion of the receptor includes two tyrosine kinase subdomains.

RET signaling is mediated by the binding of a group of soluble proteins of the glial cell line-derived neurotrophic factor (GDNF) family ligands (GFLs), which also includes neurturin (NTRN), artemin (ARTN) and persephin (PSPN) (Arighi et al., Cytokine Growth Factor Rev., 2005, 16, 441-67). Unlike other receptor tyrosine kinases, RET does not directly bind to GFLs and requires an additional co-receptor: that is, one of four GDNF family receptor-α (GFRα) family members, which are tethered to the cell surface by a glycosylphosphatidylinositol linkage. GFLs and GFRα family members form binary complexes that in turn bind to RET and recruit it into cholesterol-rich membrane subdomains, which are known as lipid rafts, where RET signaling occurs.

Upon binding of the ligand-co-receptor complex, RET dimerization and autophosphorylation on intracellular tyrosine residues recruits adaptor and signaling proteins to stimulate multiple downstream pathways. Adaptor protein binding to these docking sites leads to activation of Ras-MAPK and PI3K-Akt/mTOR signaling pathways or to recruitment of the CBL family of ubiquitin ligases that functions in RET downregulation of the RET-mediated functions.

Aberrant RET expression and/or activity have been demonstrated in different cancers and in gastrointestinal disorders such as irritable bowel syndrome (IBS).

SUMMARY OF THE INVENTION

It has now been found that substituted pyrazolo[1,5-a]pyrazine compounds are inhibitors of RET kinase, which are useful for treating diseases such as proliferative diseases such as cancers.

Accordingly, provided herein is a compound of the Formula I:

or pharmaceutically acceptable salt or solvate thereof, wherein A, B, D, E, X¹, X², X³ and X⁴ are as defined herein.

Also provided herein is a pharmaceutical composition comprising a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof, in admixture with a pharmaceutically acceptable diluent or carrier.

Also provided herein is a method of inhibiting cell proliferation, in vitro or in vivo, the method comprising contacting a cell with an effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof, or a pharmaceutical composition thereof as defined herein.

Also provided herein is a method of treating a RET-associated disease or disorder in a patient in need of such treatment, the method comprising administering to the patient a therapeutically effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof, or a pharmaceutical composition thereof as defined herein.

Also provided herein is a method of treating cancer and/or inhibiting metastasis associated with a particular cancer in a patient in need of such treatment, the method comprising administering to the patient a therapeutically effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof or a pharmaceutical composition thereof as defined herein.

Also provided herein is a method of treating irritable bowel syndrome (IBS) and/or pain associated with IBS in a patient in need of such treatment, the method comprising administering to the patient a therapeutically effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof or a pharmaceutical composition thereof as defined herein.

Also provided is a method of providing supportive care to a cancer patient, including preventing or minimizing gastrointestinal disorders, such as diarrhea, associated with treatment, including chemotherapeutic treatment, the method comprising administering to the patient a therapeutically effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof or a pharmaceutical composition thereof as defined herein.

Also provided herein is a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof, or a pharmaceutical composition thereof as defined herein for use in therapy.

Also provided herein is a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof or a pharmaceutical composition thereof as defined herein for use in the treatment of cancer and/or inhibiting metastasis associated with a particular cancer.

Also provided herein is a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof or a pharmaceutical composition thereof as defined herein for use in the treatment of irritable bowel syndrome (IBS) or pain associated with IBS.

Also provided is a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof or a pharmaceutical composition thereof as defined herein for use providing supportive care to a cancer patient, including preventing or minimizing gastrointestinal disorders, such as diarrhea, associated with treatment, including chemotherapeutic treatment.

Also provided herein is a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof for use in the inhibition of RET kinase activity.

Also provided herein is a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof or a pharmaceutical composition thereof as defined herein, for use in the treatment of a RET-associated disease or disorder.

Also provided herein is the use of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof, as defined herein in the manufacture of a medicament for the treatment of cancer and/or inhibiting metastasis associated with a particular cancer.

Also provided herein is the use of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof, as defined herein in the manufacture of a medicament for the treatment of irritable bowel syndrome (IBS) or pain associated with IBS.

Also provided herein is the use of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof, as defined herein in the manufacture of a medicament for providing supportive care to a cancer patient, including preventing or minimizing gastrointestinal disorders, such as diarrhea, associated with treatment, including chemotherapeutic treatment.

Also provided herein is a use of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof, as defined herein in the manufacture of a medicament for the inhibition of RET kinase activity.

Also provided herein is the use of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof, as defined herein, in the manufacture of a medicament for the treatment of a RET-associated disease or disorder.

Also provided herein is a method for treating cancer in a patient in need thereof, the method comprising (a) determining if the cancer is associated with a dysregulation of a RET gene, a RET kinase, or expression or activity or level of any of the same (e.g., a RET-associated cancer); and (b) if the cancer is determined to be associated with a dysregulation of a RET gene, a RET kinase, or expression or activity or level of any of the same (e.g., a RET-associated cancer), administering to the patient a therapeutically effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof, or a pharmaceutical composition thereof.

Also provided herein is a pharmaceutical combination for treating cancer (e.g., a RET-associated cancer, such as a RET-associated cancer having one or more RET inhibitor resistance mutations) in a patient in need thereof, which comprises (a) a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof, (b) an additional therapeutic agent, and (c) optionally at least one pharmaceutically acceptable carrier, wherein the compound of Formula I or the pharmaceutically acceptable salt or solvate thereof and the additional therapeutic are formulated as separate compositions or dosages for simultaneous, separate or sequential use for the treatment of cancer, wherein the amounts of the compound of Formula I or a pharmaceutically acceptable salt or solvate thereof and of the additional therapeutic agent are together effective in treating the cancer. Also provided herein is a pharmaceutical composition comprising such a combination. Also provided herein is the use of such a combination for the preparation of a medicament for the treatment of cancer. Also provided herein is a commercial package or product comprising such a combination as a combined preparation for simultaneous, separate or sequential use; and to a method of treatment of cancer a patient in need thereof.

Also provided herein is a method for reversing or preventing acquired resistance to an anticancer drug, comprising administering a therapeutically effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof, to a patient at risk for developing or having acquired resistance to an anticancer drug. In some embodiments, the patient is administered a dose of the anticancer drug (e.g., at substantially the same time as a dose of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof is administered to the patient).

Also provided herein is a method of delaying and/or preventing development of cancer resistant to an anticancer drug in an individual, comprising administering to the individual an effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof, before, during, or after administration of an effective amount of the anticancer drug.

Also provided herein is a method of treating an individual with cancer who has an increased likelihood of developing resistance to an anticancer drug, comprising administering to the individual (a) an effective amount of a compound of Formula I before, during, or after administration of (b) an effective amount of the anticancer drug.

Also provided are methods of treating an individual with a RET-associated cancer that has one or more RET inhibitor resistance mutations that increase resistance of the cancer to a first RET inhibitor (e.g., one or more amino acid substitutions in the kinase domain (e.g., amino acid positions 723 to 1012 in a wildtype RET protein), a gatekeeper amino acid (e.g., amino acid position 804 in a wildtype RET protein), the P-loop (e.g., amino acid positions 730-737 in a wildtype RET protein), the DFG motif (e.g., amino acid positions 892-894 in a wildtype RET protein), ATP cleft solvent front amino acids (e.g., amino acid positions 758, 811, and 892 in a wildtype RET protein), the activation loop (e.g., amino acid positions 891-916 in a wildtype RET protein), the C-helix and loop preceeding the C-helix (e.g., amino acid positions 768-788 in a wildtype RET protein), and/or the ATP binding site (e.g., amino acid positions 730-733, 738, 756, 758, 804, 805, 807, 811, 881, and 892 in a wildtype RET protein) (e.g., a substitution at amino acid position 804, e.g., V804M, V804L, or V804E, and/or one or more RET inhibitor resistance mutations listed in Tables 3 and 4), that include administering a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof, before, during, or after administration of another anticancer drug (e.g., a second RET kinase inhibitor). See also J. Kooistra, G. K. Kanev, O. P. J. Van Linden, R. Leurs, I. J. P. De Esch, and C. De Graaf, “KLIFS: A structural kinase-ligand interaction database,” Nucleic Acids Res., vol. 44, no. D1, pp. D365-D371, 2016; and O. P. J. Van Linden, A. J. Kooistra, R. Leurs, I. J. P. De Esch, and C. De Graaf, “KLIFS: A knowledge-based structural database to navigate kinase-ligand interaction space,” J. Med. Chem., vol. 57, no. 2, pp. 249-277, 2014, both of which are incorporated by reference in their entirety herein. In some embodiments, a wildtype RET protein is the exemplary wildtype RET protein described herein.

Also provided are methods of treating an individual with a RET-associated cancer that include administering a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof, before, during, or after administration of another anticancer drug (e.g., a first RET kinase inhibitor).

Also provided herein is a method for treating irritable bowel syndrome (IBS) in a patient in need thereof, the method comprising (a) determining if the IBS is associated with a dysregulation of a RET gene, a RET kinase, or expression or activity or level of any of the same; and (b) if the IBS is determined to be associated with a dysregulation of a RET gene, a RET kinase, or expression or activity or level of any of the same, administering to the patient a therapeutically effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof, or a pharmaceutical composition thereof.

Also provided herein is a pharmaceutical combination for treating irritable bowel syndrome (IBS) in a patient in need thereof, which comprises administering (a) a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof, (b) an additional therapeutic agent, and (c) optionally at least one pharmaceutically acceptable carrier, for simultaneous, separate or sequential use for the treatment of IBS, wherein the amounts of the compound of Formula I or a pharmaceutically acceptable salt or solvate thereof and of the additional therapeutic agent are together effective in treating the IBS. Also provided herein is a pharmaceutical composition comprising such a combination. Also provided herein is the use of such a combination for the preparation of a medicament for the treatment of the IBS. Also provided herein is a commercial package or product comprising such a combination as a combined preparation for simultaneous, separate or sequential use; and to a method of treatment of the IBS a patient in need thereof.

Also provided herein is a process for preparing a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof.

Also provided herein is a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof obtained by a process of preparing the compound as defined herein.

Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. Methods and materials are described herein for use in the present invention; other, suitable methods and materials known in the art can also be used. The materials, methods, and examples are illustrative only and not intended to be limiting. All publications, patent applications, patents, sequences, database entries, and other references mentioned herein are incorporated by reference in their entirety. In case of conflict, the present specification, including definitions, will control.

Other features and advantages of the invention will be apparent from the following detailed description and figures, and from the claims.

DETAILED DESCRIPTION OF THE INVENTION

Provided herein is a compound of the Formula I:

or a pharmaceutically acceptable salt or solvate thereof, wherein:

X¹ is CH, CCH₃, CF, CCl or N;

X² is CH, CF or N;

X³ is CH, CF or N;

X⁴ is CH, CF or N;

wherein zero, one or two of X¹, X², X³ and X⁴ is N;

A is H, Cl, CN, Br, CH₃, CH₂CH₃ or cyclopropyl;

B is hetAr¹;

hetAr¹ is a 5-membered heteroaryl ring having 1-3 ring heteroatoms independently selected from N, S and O, wherein the heteroaryl ring is optionally substituted with one or more substituents independently selected from the group consisting of halogen, C1-C6 alkyl (optionally substituted with one to three fluoros), hydroxyC1-C6 alkyl-, cyanoC1-C6 alkyl-(C1-C6 alkoxy)C1-C6 alkyl-, (C1-C4 alkoxy)CH₂C(═O)—, (C1-C4 alkoxy)C(═O)C1-C3 alkyl-, C3-C6 cycloalkyl, (R^(a)R^(b)N)C1-C6 alkyl-, (R^(a)R^(b)N)C(═O)C1-C6 alkyl-, (C1-C6 alkylSO₂)C1-C6 alkyl-, hetCyc^(a), hetCyc^(a)C1-C6 alkyl-, and 4-methoxybenzyl;

R^(a) and R^(b) are independently H or C1-C6 alkyl;

hetCyc^(a) is a 4-6 membered heterocyclic ring having a ring heteroatom selected from N and O, wherein the heterocyclic ring is optionally substituted with halogen, C1-C6 alkyl (optionally substituted with one to three fluoros), (C1-C6 alkoxy)C1-C6 alkyl-, di(C1-C3 alkyl)NCH₂C(═O)—, (C1-C6 alkoxy)C(═O)— or (C1-C6 alkoxy)CH₂C(═O)—;

D is hetCyc¹, hetCyc², hetCyc³ or hetCyc⁹;

hetCyc¹ is a 4-6 membered heterocyclic ring having 1-2 ring atoms independently selected from N and O, wherein the heterocyclic ring is optionally substituted with one or more substituents independently selected from the group consisting of C1-C3 alkyl (optionally substituted with one to three fluoros), and OH, or said heterocyclic ring is substituted with a C3-C6 cycloalkylidene ring, or said heterocyclic ring is substituted with an oxo group;

hetCyc² is a 7-8 membered bridged heterocyclic ring having 1-3 ring heteroatoms independently selected from N and O, wherein the heterocyclic ring is optionally substituted with one or more substituents independently selected from the group consisting of C1-C3 alkyl;

hetCyc³ is a 7-11 membered heterospirocyclic ring having 1-2 ring heteroatoms independently selected from N and O, wherein the ring is optionally substituted with C1-C3 alkyl;

hetCyc⁹ is a fused 9-10 membered heterocyclic ring having 1-3 ring nitrogen atoms, wherein the heterocyclic ring is optionally substituted with oxo;

E is

(a) hydrogen,

(b) OH,

(c) R′R″N(CH₂)_(n)— wherein R′ is H or C1-C6 alkyl, R″ is H, C1-C6 alkyl or phenyl, and n is 0 or 1;

(d) C1-C6 alkyl optionally substituted with one to three fluoros,

(e) hydroxyC1-C6 alkyl- optionally substituted with one to three fluoros,

(f) C1-C6 alkoxy optionally substituted with one to three fluoros,

(g) hydroxyC1-C6 alkoxy- optionally substituted with one to three fluoros,

(h) (C1-C6 alkoxy)hydroxy C1-C6 alkyl- optionally substituted with one to three fluoros,

(i) (C1-C6 alkyl)C(═O)—, wherein said alkyl portion is optionally substituted with one to three fluoros, or said alkyl portion is substituted with R′R″N— or R′R″NCH₂— wherein R′ and R″ are independently H or C1-C6 alkyl,

(j) (hydroxy C1-C6 alkyl)C(═O)— optionally substituted with one to three fluoros,

(k) (C1-C6 alkoxy)C(═O)—,

(l) (C1-C6 alkoxy)(C1-C6 alkyl)C(═O)—,

(m) HC(═O)—,

(n) Cyc¹,

(o) Cyc¹C(═O)—,

(p) Cyc¹(C1-C6 alkyl)C(═O)— wherein the alkyl portion is optionally substituted with one or more groups independently selected from the group consisting of OH, fluoro, C1-C3 alkoxy and R^(c)R^(d)N—, where R^(c) and R^(d) are independently H or C1-C6 alkyl,

(q) hetCyc⁴,

(r) hetCyc⁴C(═O)—,

(s) hetCyc⁴(C1-C6 alkyl)C(═O)—,

(t) hetCyc⁴C(═O)C1-C6 alkyl-,

(u) hetCyc⁴C(═O)NR^(g)—, where R^(g) is H or C1-C6 alkyl,

(v) Ar²,

(w) Ar²C(═O)—,

(x) (Ar²)C1-C6 alkyl-,

(y) (Ar²)hydroxy C2-C6 alkyl-,

(z) Ar²(C1-C6 alkyl)C(═O)— wherein the alkyl portion is optionally substituted with one or two groups independently selected from the group consisting of OH, C1-C6 alkyl (optionally substituted with 1-3 fluoros), hydroxyC1-C6 alkyl, C1-C6 alkoxy, R^(e)R^(f)N— and (R^(e)R^(f)N)C1-C3 alkyl- wherein R^(e) and R^(f) are independently H or C1-C6 alkyl, or said alkyl portion is substituted with a 5-6 membered heterocyclic ring having one or two ring heteroatoms independently selected from N and O and wherein the heterocyclic ring is optionally substituted with C1-C6 alkyl,

(aa) hetAr²C(═O)—,

(bb) (hetAr²)hydroxyC2-C6 alkyl-,

(cc) hetAr²(C1-C6 alkyl)C(═O)— wherein the alkyl portion is optionally substituted with one or two groups independently selected from the group consisting of OH, C1-C6 alkyl, hydroxyC1-C6 alkyl, C1-C6 alkoxy, R^(e)R^(f)N— and (R^(e)R^(f)N)C1-C3 alkyl-, wherein R^(e) and R^(f) are independently H or C1-C6 alkyl, or said alkyl portion is substituted with a 5-6 membered heterocyclic ring having one or two ring heteroatoms independently selected from N and O, wherein the heterocyclic ring is optionally substituted with C1-C6 alkyl,

(dd) R¹R²NC(═O)—,

(ee) R¹R²N(C1-C6 alkyl)C(═O)— wherein the alkyl portion is optionally substituted with phenyl,

(ff) R¹R²NC(═O)C1-C6 alkyl-,

(gg) R¹R²NC(═O)NH—,

(hh) CH₃SO₂(C1-C6 alkyl)C(═O)—,

(ii) (C1-C6 alkyl)SO₂—,

(jj) (C3-C6 cycloalkyl)CH₂SO₂—,

(kk) hetCyc⁵-SO₂—,

(ll) R⁴R⁵NSO₂—,

(mm) R⁶C(═O)NH—,

(nn) hetCyc⁶;

(oo) hetAr²C1-C6 alkyl-,

(pp) (hetCyc⁴)C1-C6 alkyl-,

(qq) (C1-C6 alkoxy)C1-C6 alkyl- wherein said alkoxy portion is optionally substituted with 1-3 fluoros,

(rr) (C3-C6 cycloalkoxy)C1-C6 alkyl-,

(ss) (C3-C6 cycloalkyl)C1-C6 alkyl- wherein said cycloalkyl is optionally substituted with 1-2 fluoros,

(tt) (R^(g)R^(h)N)C1-C6 alkyl- wherein R^(g) and R^(h) are independently H or C1-C6 alkyl,

(uu) Ar²—O—,

(vv) (C1-C6 alkylSO₂)C1-C6 alkyl-,

(ww) (C1-C6 alkoxy)C(═O)NHC1-C6 alkyl-,

(xx) (C3-C6 cycloalkoxy)C(═O)—,

(yy) (C3-C6 cycloalkyl)SO₂— wherein said cycloalkyl is optionally substituted with C1-C6 alkyl,

(zz) Ar⁴CH₂OC(═O)—,

(aaa) (N—(C1-C3 alkyl)pyridinonyl)C1-C6 alkyl-,

(bbb) (Ar⁴SO₂)C1-C6 alkyl-, and

(ccc) (hetAr²)—O—;

Cyc¹ is a C3-C6 cycloalkyl, wherein (a) the cycloalkyl is optionally substituted with one or more substituents independently selected from the group consisting of OH, halogen, C1-C6 alkoxy, CN, hydroxyC1-C6 alkyl-, (C1-C6 alkoxy)C1-C6 alkyl-, and C1-C6 alkyl optionally substituted with 1-3 fluoros, or (b) the cycloalkyl is substituted with phenyl, wherein the phenyl is optionally substituted with one or more substituents independently selected from the group consisting of halogen, C1-C3 alkyl, C1-C3 alkoxy and CF₃, or (c) the cycloalkyl is substituted with a 5-6 membered heteroaryl ring having 1-3 ring heteroatoms independently selected from N and O, wherein the heteroaryl ring is optionally substituted with one or more substituents independently selected from the group consisting of halogen, C1-C3 alkyl, C1-C3 alkoxy and CF₃;

Ar² is phenyl optionally substituted with one or more substituents independently selected from the group consisting of halogen, C1-C6 alkyl (optionally substituted with one to three fluoros), C1-C6 alkoxy (optionally substituted with 1-3 fluoros), CN, a 5-6 membered heterocyclic ring having 1-2 ring heteroatoms independently selected from N and O, and R^(i)R^(j)N— where R^(i) and R^(j) are independently selected from H and C1-C6 alkyl;

hetAr² is a 5-6 membered monocyclic heteroaryl ring having 1-3 ring heteroatoms independently selected from N, O and S or a 9-10 membered bicyclic heteroaryl ring having 1-2 ring nitrogen atoms, wherein hetAr² is optionally substituted with one or more substituents independently selected from the group consisting of halogen, C1-C6 alkyl (optionally substituted with one to three fluoros), C1-C6 alkoxy (optionally substituted with 1-3 fluoros), hydroxyC1-C6 alkyl, (C3-C6)cycloalkyl, (C1-C6 alkoxy)C1-C6 alkyl-, CN and R′R″N— where R′ and R″ are independently H or C1-C3 alkyl;

hetCyc⁴ is (a) a 4-6 membered heterocyclic ring having 1-2 ring heteroatoms independently selected from N, O and S wherein said S is optionally oxidized to SO₂, (b) a 7-8 membered bridged heterocyclic ring having 1-2 ring heteroatoms independently selected from N and O, (c) a 6-12 membered fused bicyclic heterocyclic ring having 1-2 ring heteroatoms independently selected from N and O, wherein the heterocyclic ring is optionally independently substituted with one to two C1-C6 alkyl substituents, or (d) a 7-10 membered spirocyclic heterocyclic ring having 1-2 ring heteroatoms independently selected from N and O, wherein each of the heterocyclic rings is optionally substituted with one or more substituents independently selected from the group consisting of halogen, OH, CN, C1-C6 alkyl (optionally substituted with 1-3 fluoros), C1-C6 alkoxy, (C1-C6 alkoxy)C1-C6 alkyl-, (C3-C6)cycloalkyl, (C1-C6 alkyl)C(═O)—, a 5-6 membered heterocyclic ring having 1-2 ring heteroatoms independently selected from N and O, and phenyl wherein said phenyl is optionally substituted with one or more substituents independently selected from halogen, C1-C6 alkyl and C1-C6 alkoxy;

hetCyc⁵ is a 5-6 membered heterocyclic ring having a ring heteroatom selected from O and N;

hetCyc⁶ is a 5 membered heterocyclic ring having one or two ring heteroatoms independently selected from N and O, wherein the ring substituted with oxo and wherein the ring is further optionally substituted with one or more substituents independently selected from the group consisting of OH and C1-C6 alkyl;

R¹ is H, C1-C6 alkyl or (C1-C6 alkoxy)C1-C6 alkyl-;

R² is H, C1-C6 alkyl (optionally substituted with 1-3 fluoros), (C1-C6 alkoxy)C1-C6 alkyl-(optionally substituted with 1-3 fluoros), Cyc³, hydroxyC1-C6 alkyl (optionally substituted with 1-3 fluoros), C1-C6 alkoxy (optionally substituted with 1-3 fluoros), (C1-C6 alkoxy)C(═O), hetCyc⁷, Ar³, Ar³C1-C3 alkyl-, hydroxyC1-C6 alkoxy or (C3-C6 cycloalkyl)CH₂O—;

Cyc³ is a 3-6 membered carbocyclic ring optionally substituted with 1-2 groups independently selected from the group consisting of C1-C6 alkoxy, OH and halogen;

hetCyc⁷ is a 5-6 membered heterocyclic ring having a ring heteroatom selected from O and N wherein the ring is optionally substituted with C1-C6 alkyl;

Ar³ is phenyl optionally substituted with one or more substituents independently selected from halogen, C1-C3 alkyl (optionally substituted with one to three fluoros), and C1-C3 alkoxy;

R⁴ and R⁵ are independently H or C1-C6 alkyl;

R⁶ is C1-C6 alkyl, hydroxyC1-C6 alkyl, C1-C6 alkoxy, (C1-C6 alkoxy)C1-C6 alkyl-, phenyl or hetCyc⁸;

hetCyc⁸ is a 5-6 membered heterocyclic ring having a ring heteroatom selected from O and N, wherein the heterocyclic ring is optionally substituted with C1-C6 alkyl; and

Ar⁴ is phenyl optionally substituted with one or more halogens.

As used herein, the word “a” before a noun represents one or more of the particular noun. For example, the phrase “a cell” represents “one or more cells.”

For complex chemical names employed herein, a substituent group is typically named before the group to which it attaches. For example, methoxyethyl group comprises an ethyl backbone with a methoxy substituent.

The term “halogen” means —F (sometimes referred to herein as “fluoro” or “fluoros”), —Cl, —Br and —I.

The term “azacyclic ring” as used herein refers to a saturated heterocyclic ring having one ring nitrogen atom.

The terms “C1-C3 alkyl” and “C1-C6 alkyl” as used herein refer to saturated linear or branched-chain monovalent hydrocarbon radicals of one to three or one to six carbon atoms, respectively. Examples include, but are not limited to, methyl, ethyl, 1-propyl, isopropyl, 1-butyl, isobutyl, sec-butyl, tert-butyl, 2-methyl-2-propyl, pentyl, and hexyl. A C1-C3 alkyl or C1-C6 alkyl optionally substituted with 1-3 fluoros includes, but is not limited to, fluoromethyl, 3-fluoromethyl, 2-fluoroethyl, difluoromethyl, 2,2,fluoromethyl, 1,3-difluoroprop-2-yl, trifluoromethyl, 2,2,2-trifluoroethyll and 3,3,3-trifluoropropyl.

The terms “C1-C3 alkoxy”, “C1-C4 alkoxy” and “C1-C6 alkoxy”, as used herein refer to saturated linear or branched-chain monovalent alkoxy radicals of one to three, one to four or one to six carbon atoms, respectively, wherein the radical is on the oxygen atom. Examples include methoxy, ethoxy, propoxy, isopropoxy, and butoxy.

The term “(C1-C6 alkoxy)C1-C6 alkyl-” as used herein refers to saturated linear or branched-chain monovalent radicals of one to six carbon atoms, wherein one of the carbon atoms is substituted with a (C1-C6 alkoxy) group as defined herein. Examples include methoxymethyl (CH₃OCH₂—) and methoxyethyl (CH₃OCH₂CH₂—).

The term “hydroxyC1-C6 alkyl” as used herein refers to saturated linear or branched-chain monovalent alkyl radicals of one to six carbon atoms, wherein one of the carbon atoms is substituted with a hydroxy group.

The term “hydroxyC1-C6 alkoxy” as used herein refers to saturated linear or branched-chain monovalent alkoxy radicals of one to six carbon atoms, wherein one of the carbon atoms is substituted with a hydroxy group.

The term “(C1-C6 alkoxy)hydroxyC1-C6 alkyl” as used herein refers to a hydroxy (C1-C6 alkyl) radical as defined herein, wherein one of the carbon atoms is substituted with a C1-C6 alkoxy group as defined herein.

The term “Cyc¹(C1-C6 alkyl)” as used herein refers to saturated linear or branched-chain monovalent alkyl radicals of one to six carbon atoms, wherein one of the carbon atoms is substituted with a 3-6 membered cycloalkyl ring.

The term “Cyc¹(C1-C6 alkyl)C(═O)—” as used herein refers to a (C1-C6 alkyl)C(═O)— group, wherein the C1-C6 alkyl is a saturated linear or branched-chain monovalent radical of one to six carbon atoms and wherein one of the carbon atoms of the C1-C6 alkyl portion is substituted with a C3-C6 cycloalkyl group.

The term “Ar²C1-C6 alkyl” as used herein refers to C1-C6 alkyl radical as defined herein one of the carbon atoms of the alkyl portion is substituted with Ar².

The term “(Ar²)hydroxy C2-C6 alkyl” as used herein refers to a hydroxyC1-C6 alkyl radical as defined herein wherein one of the carbon atoms of the alkyl portion is substituted with Ar².

The term “Ar²(C1-C6 alkyl)C(═O)—” as used herein refers to a C1-C6 alkyl(C═O)— radical wherein the C1-C6 alkyl portion is a saturated linear or branched-chain monovalent alkyl radicals of one to three carbon atoms, wherein one of the carbon atoms is substituted with Ar².

The term “(hetAr²)hydroxy C2-C6 alkyl” as used herein refers to a hydroxyC2-C6 alkyl radical as defined herein wherein one of the carbon atoms is substituted with hetAr².

The term “hetAr²(C1-C6 alkyl)C(═O)—” as used herein refers to a C1-C6 alkyl(C═O)— radical wherein the C1-C6 alkyl portion is a saturated linear or branched-chain monovalent alkyl radical of one to three carbon atoms, wherein one of the carbon atoms is substituted with hetAr².

The term “R¹R²NC(═O)C1-C6 alkyl” as used herein refers to a C1-C6 alkyl radical wherein one of the carbon atoms is substituted with a R¹R²NC(═O)— group.

The term “R¹R²N(C1-C6 alkyl)C(═O)—” as used herein refers to a C1-C3 alkyl(C═O)— radical wherein the C1-C6 alkyl portion is a saturated linear or branched-chain monovalent alkyl radicals of one to three carbon atoms, wherein one of the carbon atoms is substituted with a R¹R²N— group, wherein R¹ and R² are as defined for Formula I.

The term “(C1-C6 alkylSO₂)C1-C6 alkyl” as used herein as used herein refers to saturated linear or branched-chain monovalent radicals of one to six carbon atoms, wherein one of the carbon atoms is substituted with a (C1-C6 alkyl)SO₂— group (e.g., a (CH₃)₂CH₂SO₂— group).

The term “(Ar⁴SO₂)C1-C6 alkyl” as used herein as used herein refers to saturated linear or branched-chain monovalent radicals of one to six carbon atoms, wherein one of the carbon atoms is substituted with a (Ar⁴)SO₂— group.

The term “bridged heterocyclic ring” as used herein refers to a bicyclic heterocycle, wherein two common nonadjacent carbon atoms of the ring are linked by an alkylene bridge of 1, 2, 3, or 4 carbon atoms. Examples of bridged heterocyclic ring systems include 3,6-diazabicyclo[3.1.1]heptane, 2,5-diazabicyclo[2.2.1]heptane, 3,8-diazabicyclo[3.2.1]octane, 3,8-diazabicyclo[3.2.1]octane, 8-azabicyclo[3.2.1]octane and 7-azabicyclo[2.2.1]heptane.

The term “spirocyclic ring” as used herein refers to a group having two rings joined by a spirocyclic linkage through a common single carbon atom, wherein each ring is a 4-7-membered ring (including the common carbon atom).

The term “heterospirocyclic” as used herein refers to a group having two rings joined by a spirocyclic linkage through a carbon atom, wherein each ring has 4 to 6 ring atoms (with one ring atom being common to both rings), and wherein 1 or 2 of the ring atoms is a heteroatom selected from the group consisting of N and O, provided that the heteroatoms are not adjacent. Examples include 2,6-diazaspiro[3.3]heptane, 2,5-diazaspiro[3.4]octane, 2,6-diazaspiro[3.4]octane, 6-oxa-2-azaspiro[3.4]octane, 2-oxa-7-azaspiro[4.4]nonane, 7-oxa-2-azaspiro[4.5]decane, 7-oxa-2-azaspiro[3.5]nonane, 2,7-diazaspiro[3.5]nonane, 2,6-diazaspiro[3.5]nonane, 2,5-diazaspiro[3.5]nonane, 1,6-diazaspiro[3.4]octane, 1,7-diazaspiro[4.4]nonane, 2,7-diazaspiro[4.4]nonane, 2,8-diazaspiro[4.5]decane, 2,7-diazaspiro[4.5]decane, 2,6-diazaspiro[4.5]decane, 1,7-diazaspiro[3.5]nonane, 2,7-diazaspiro[3.5]nonane, 1,6-diazaspiro[3.5]nonane, 1,8-diazaspiro[4.5]decane, 2,8-diazaspiro[4.5]decane, 2,7-diazaspiro[4.5]decane, 1,7-diazaspiro[4.5]decane, 2,9-diazaspiro[5.5]undecane, and 7-azaspiro[3.5]nonane.

As used herein, the term “cycloalkylidine ring” refers to a divalent carbocyclic ring. The suffix “ylidine” refers to bivalent radical derived from a saturated hydrocarbon by removal of two hydrogen atoms from the same carbon atom.

The term “compound,” as used herein is meant to include all stereoisomers, geometric isomers, tautomers, and isotopes of the structures depicted. Compounds herein identified by name or structure as one particular tautomeric form are intended to include other tautomeric forms unless otherwise specified.

The term “tautomer” as used herein refers to compounds whose structures differ markedly in arrangement of atoms, but which exist in easy and rapid equilibrium, and it is to be understood that compounds provided herein may be depicted as different tautomers, and when compounds have tautomeric forms, all tautomeric forms are intended to be within the scope of the invention, and the naming of the compounds does not exclude any tautomer.

The term “oxo” as used herein means an oxygen that is double bonded to a carbon atom. For example, a non-limiting example of a heterocyclic ring that is substituted with an oxo group is the structure:

The term “(N—(C1-C3 alkyl)pyridinonyl)C1-C6 alkyl” as used herein refers to a C1-C6 alkyl radical as defined herein where one of the carbon atoms of the alkyl portion is substituted with a 2-oxo-1,2-dihydropyridine that is substituted on the pyridone nitrogen with 1-3 carbons. Examples include 1-methyl-1,2-dihydropyridin-2-one.

In one embodiment of Formula I, X¹ is CH, CCH₃, CF, or CCl, X² is CH or CF, X³ is CH or CF, and X⁴ is CH or CF. In one embodiment, X¹ is CH or CH₃, X² is CH, X³ is CH, and X³ is CH. In one embodiment, each of X¹, X², X³ and X⁴ is CH.

In one embodiment of Formula I, X¹ is CH, CCH₃, CF, CCl or N, X² is CH, CF or N, X³ is CH, CF or N, and X⁴ is CH, CF or N, wherein one of X¹, X², X³ and X⁴ is N.

In one embodiment, X¹ is N, CH or CH₃, X² is CH or N, X³ is CH or N, and X³ is CH or N, wherein one of X¹, X², X³ and X⁴ is N.

In certain embodiments of Formula I, X¹ is N, X² is CH or CF, X³ is CH or CF, and X⁴ is CH or CF. In one embodiment, X¹ is N, and X², X³ and X⁴ are CH.

In one embodiment of Formula I, X¹ is CCH₃, X² is CH, CF or N; X³ is CH, CF or N, and X⁴ is CH, CF or N; wherein one of X², X³ and X⁴ is N. In one embodiment, X¹ is CCH₃, X² is N; X³ is CH or CF, and X⁴ is CH or CF. In one embodiment, X¹ is CCH₃, X² is N, and X³ and X⁴ are CH.

In one embodiment of Formula I, X¹ is CH, CCH₃, CF, CCl or N; X² is CH, CF or N; X³ is CH, CF or N; and X⁴ is CH, CF or N, wherein two of X¹, X², X³ and X⁴ are N.

In one embodiment of Formula I, X¹ and X² are N, and X³ and X⁴ are CH or CF. In one embodiment, X¹ and X² are N, and X³ and X⁴ are CH.

In one embodiment, X¹ and X³ are N, and X² and X⁴ are CH or CF. In one embodiment, X¹ and X³ are N, and X² and X⁴ are CH.

In one embodiment, A is H.

In one embodiment, A is Cl.

In one embodiment, A is CN.

In one embodiment, A is Br.

In one embodiment, A is CH₃.

In one embodiment, A is CH₃CH₂—.

In one embodiment, A is cyclopropyl.

In one embodiment, A is H, Cl or CN.

In one embodiment, hetAr¹ is pyrazolyl, imidazolyl, oxazolyl, isoxazolyl thiazolyl, thiadiazolyl, triazolyl or oxadiazolyl optionally substituted with one or more substituents independently selected from the group consisting of halogen, C1-C6 alkyl (optionally substituted with one to three fluoros), hydroxyC1-C6 alkyl-, cyanoC1-C6 alkyl- (C1-C6 alkoxy)C1-C6 alkyl-, (C1-C4 alkoxy)CH₂C(═O)—, (C1-C4 alkoxy)C(═O)C1-C3 alkyl-, C3-C6 cycloalkyl, (R^(a)R^(b)N)C1-C6 alkyl-, (R^(a)R^(b)N)C(═O)C1-C6 alkyl-, (C1-C6 alkylSO₂)C1-C6 alkyl-, hetCyc^(a), hetCyc^(a)C1-C6 alkyl-, and 4-methoxybenzyl.

In one embodiment, B is hetAr¹, where hetAr¹ is a 5 membered heteroaryl having 1-2 ring heteroatoms independently selected from N, O and S and optionally substituted with one or more substituents independently selected from the group consisting of C1-C6 alkyl (optionally substituted with one to three fluoros), (C1-C6 alkoxy)C1-C6 alkyl-, (C1-C6 alkylSO₂)C1-C6 alkyl-, hetCyc^(a), and hetCyc^(a)C1-C6 alkyl. In one embodiment, hetAr¹ is pyrazolyl optionally substituted with one or more substituents independently selected from the group consisting of C1-C6 alkyl (optionally substituted with one to three fluoros), (C1-C6 alkoxy)C1-C6 alkyl-, (C1-C6 alkylSO₂)C1-C6 alkyl-, hetCyc^(a), and hetCyc^(a)C1-C6 alkyl.

In one embodiment, B is hetAr¹, wherein hetAr¹ is a pyrazolyl ring optionally substituted with one or more substituents independently selected from the group consisting of C1-C6 alkyl (optionally substituted with one to three fluoros).

In one embodiment, B is pyrazolyl optionally substituted with one or more substituents independently selected from the group consisting of C1-C6 alkyl (optionally substituted with one to three fluoros) and hydroxyC1-C6 alkyl-.

In one embodiment, B is pyrazolyl optionally substituted with one or more independently selected C1-C6 alkyl substituents.

Non-limiting examples of hetAr¹ include the structures:

In one embodiment, D is hetCyc¹ where hetCyc¹ is a 4-6 membered heterocyclic ring having 1-2 ring atoms independently selected from N and O, wherein the heterocyclic ring is optionally substituted with one or more substituents independently selected from the group consisting of C1-C3 alkyl (optionally substituted with one to three fluoros) and OH, or the heterocyclic ring is substituted with a C3-C6 cycloalkylidene ring, or the heterocyclic ring is substituted with an oxo group.

In one embodiment, hetCyc¹ is a pyrrolidinyl, piperidinyl, piperazinyl, morpholinyl or azetidinyl ring optionally substituted with one or more substituents independently selected from the group consisting of C1-C3 alkyl (optionally substituted with one to three fluoros) and OH, or hetCyc¹ is a piperazinyl ring substituted with a C3-C6 cycloalkylidene ring, or said heterocyclic ring is a piperazinyl ring substituted with an oxo group.

In one embodiment, hetCyc¹ is a 4-6 membered heterocyclic ring having one ring nitrogen atom, wherein said ring is optionally substituted with C1-C3 alkyl (optionally substituted with one to three fluoros) or OH. Non-limiting examples include the structures:

where the asterisk indicates the point of attachment to the E group and the wavy line indicates the point of attachment to the ring comprising X¹, X², X³ and X⁴, wherein X¹, X², X³, X⁴ and E are as defined for Formula I.

In one embodiment, hetCyc¹ is a 4-6 membered heterocyclic ring having one ring nitrogen atom, wherein said ring is optionally substituted with C1-C3 alkyl (optionally substituted with one to three fluoros) or OH. In one embodiment, hetCyc¹ is represented by the structures:

where the asterisk indicates the point of attachment to the E group and the wavy line indicates the point of attachment to the ring comprising X¹, X², X³ and X⁴, wherein X¹, X², X³, X⁴ and E are as defined for Formula I. In one embodiment, E is (a) hydrogen, (b) OH, (c) R′R″N(CH₂)_(n)— wherein R′ is H or C1-C6 alkyl, R″ is H, C1-C6 alkyl or phenyl, and n is 0 or 1, (f) C1-C6 alkoxy optionally substituted with one to three fluoros, (g) hydroxyC1-C6 alkoxy- optionally substituted with one to three fluoros, (k) (C1-C6 alkoxy)C(═O)—, (m) HC(═O)—, (r) hetCyc⁴C(═O)—, (u) hetCyc⁴C(═O)NR^(g)—, where R^(g) is H or C1-C6 alkyl, (v) Ar², (x) (Ar²)C1-C6 alkyl-, (dd) R¹R²NC(═O)—, (ff) R¹R²NC(═O)C1-C6 alkyl-, (gg) R¹R²NC(═O)NH—, (II) R⁴R⁵NSO₂—, (mm) R⁶C(═O)NH—, (nn) hetCyc⁶, (oo) (hetAr²)C1-C6 alkyl-, (tt) (R^(g)R^(h)N)C1-C6 alkyl- wherein R^(g) and R^(h) are independently H or C1-C6 alkyl, (uu) Ar²—O—, or (ccc) hetAr²—O—, where hetCyc⁴, Ar², R¹, R², R⁴, R⁵, R⁶, hetCyc⁶, and hetAr² are as defined for Formula I.

In one embodiment, hetCyc¹ is a 4-6 membered heterocyclic ring having two ring nitrogen atoms, wherein said ring is optionally substituted with a C3-C6 cycloalkylidene ring or oxo. In one embodiment, hetCyc¹ is represented by the structures:

where the asterisk indicates the point of attachment to the E group and the wavy line indicates the point of attachment to the ring comprising X¹, X², X³ and X⁴, where E is as defined for Formula I. In one embodiment, E is (a) hydrogen, (d) C1-C6 alkyl optionally substituted with one to three fluoros, (e) hydroxyC1-C6 alkyl- optionally substituted with one to three fluoros, (h) (C1-C6 alkoxy)hydroxy C1-C6 alkyl-, (i) (C1-C6 alkyl)C(═O)— wherein said alkyl portion is optionally substituted with one to three fluoros, or said alkyl portion is substituted with R′R″N— or R′R″NCH₂— wherein R′ and R″ are independently H or C1-C6 alkyl, (j) (hydroxy C1-C6 alkyl)C(═O)— optionally substituted with one to three fluoros, (k) (C1-C6 alkoxy)C(═O)—, (I) (C1-C6 alkoxy)(C1-C6 alkyl)C(═O)—, (n) Cyc¹, (o) Cyc¹C(═O)—, (p) Cyc¹(C1-C6 alkyl)C(═O)— wherein the alkyl portion is optionally substituted with one or more groups independently selected from the group consisting of OH, fluoro, C1-C3 alkoxy and R^(c)R^(d)N—, where R^(c) and R^(d) are independently H or C1-C6 alkyl, (q) hetCyc⁴, (r) hetCyc⁴C(═O)—, (s) hetCyc⁴(C1-C6 alkyl)C(═O)—, (t) hetCyc⁴C(═O)C1-C6 alkyl-, (w) Ar²C(═O)—, (x) (Ar²)C1-C6 alkyl-, (y) (Ar²)hydroxy C2-C6 alkyl-, (z) Ar²(C1-C6 alkyl)C(═O)— wherein the alkyl portion is optionally substituted with one or two groups independently selected from the group consisting of OH, C1-C6 alkyl (optionally substituted with 1-3 fluoros), hydroxyC1-C6 alkyl, C1-C6 alkoxy, R^(e)R^(f)N— and (R^(e)R^(f)N)C1-C3 alkyl- wherein R^(e) and R^(f) are independently H or C1-C6 alkyl, or said alkyl portion is substituted with a 5-6 membered heterocyclic ring having one or two ring heteroatoms independently selected from N and O and wherein the heterocyclic ring is optionally substituted with C1-C6 alkyl, (aa) hetAr²C(═O)—, (bb) (hetAr²)hydroxy C2-C6 alkyl-, (cc) hetAr²(C1-C6 alkyl)C(═O)— wherein the alkyl portion is optionally substituted with one or two groups independently selected from the group consisting of OH, C1-C6 alkyl, hydroxyC1-C6 alkyl, C1-C6 alkoxy, R^(e)R^(f)N— and (R^(e)R^(f)N)C1-C3 alkyl- wherein R^(e) and R^(f) are independently H or C1-C6 alkyl, or said alkyl portion is substituted with a 5-6 membered heterocyclic ring having one or two ring heteroatoms independently selected from N and O and wherein the heterocyclic ring is optionally substituted with C1-C6 alkyl, (dd) R¹R²NC(═O)—, (ee) R¹R²N(C1-C6 alkyl)C(═O)— wherein the alkyl portion is optionally substituted with phenyl, (ff) R¹R²NC(═O)C1-C6 alkyl-, (hh) CH₃SO₂(C1-C6 alkyl)C(═O)—, (ii) (C1-C6 alkyl)SO₂—, (jj) (C3-C6 cycloalkyl)CH₂SO₂—, (kk) hetCyc⁵-SO₂—, (II) R⁴R⁵NSO₂—, (oo) (hetAr²)C1-C6 alkyl-, (pp) (hetCyc⁴)C1-C6 alkyl-, (qq) (C1-C6 alkoxy)C1-C6 alkyl- wherein said alkoxy portion is optionally substituted with 1-3 fluoros, (rr) (C3-C6 cycloalkoxy)C1-C6 alkyl-, (ss) (C3-C6 cycloalkyl)C1-C6 alkyl-, (tt) (R^(g)R^(h)N)C1-C6 alkyl- wherein R^(g) and R^(h) are independently H or C1-C6 alkyl, (vv) (C1-C6 alkyl)SO₂C1-C6 alkyl-, (ww) (C1-C6 alkoxy)C(═O)NHC1-C6 alkyl-, (yy) (C3-C6 cycloalkyl)SO₂— wherein said cycloalkyl is optionally substituted with C1-C6 alkyl, (aaa) (N—(C1-C3 alkyl)pyridinonyl)C1-C6 alkyl-, or (bbb) (Ar⁴SO₂)C1-C6 alkyl-, where Cyc¹, hetCyc⁴, Ar², hetAr², R¹, R², R⁴, R⁵ and Ar⁴ are as defined for Formula I.

In one embodiment of the D-E group, D is hetCyc¹ and E is hydrogen. In one embodiment, hetCyc¹ is a 4-6 membered heterocyclic ring having one to two ring nitrogen atoms, wherein the ring is optionally substituted with a C3-C6 cycloalkylidene ring. Non-limiting examples include the structures:

In one embodiment, D is hetCyc¹ and E is OH. In one embodiment, hetCyc¹ is a 5-6 membered heterocyclic ring having one ring nitrogen atom, wherein the ring is optionally substituted with trifluoroC1-C3 alkyl. Non-limiting examples include the structures:

In one embodiment, D is hetCyc¹ and E is R′R″N(CH₂)_(n)—, wherein R′ is H or C1-C6 alkyl, R″ is H, C1-C6 alkyl or phenyl, and n is 0 or 1. In one embodiment, hetCyc¹ is a 6 membered heterocyclic ring having one ring nitrogen atom, wherein the ring is optionally substituted with C1-C3 alkyl. Non-limiting examples include the structures:

In one embodiment of the D-E group, D is hetCyc¹ and E is C1-C6 alkyl optionally substituted with one to three fluoros. In one embodiment, hetCyc¹ is a 6-membered heterocyclic ring having two ring nitrogen atoms. Non-limiting examples include the structures:

In one embodiment, D is hetCyc¹ and E is hydroxyC1-C6 alkyl- optionally substituted with one to three fluoros. In one embodiment, hetCyc¹ is a 6-membered heterocyclic ring having two ring nitrogen atoms. Non-limiting examples include the structures:

In one embodiment, D is hetCyc¹ and E is C1-C6 alkoxy optionally substituted with one to three fluoros. In one embodiment, hetCyc¹ is a 6-membered heterocyclic ring having one ring nitrogen atom. Non-limiting examples include the structures:

In one embodiment, D is hetCyc¹ and E is hydroxyC1-C6 alkoxy- optionally substituted with one to three fluoros. In one embodiment, hetCyc¹ is a 6-membered heterocyclic ring having one ring nitrogen atom. A non-limiting examples include the structure:

In one embodiment, D is hetCyc¹ and E is (C1-C6 alkoxy)hydroxy C1-C6 alkyl- optionally substituted with one to three fluoros. In one embodiment, hetCyc¹ is a 6-membered heterocyclic ring having two ring nitrogen atoms. A non-limiting example includes the structure:

In one embodiment, D is hetCyc¹ and E is (C1-C6 alkyl)C(═O)—, wherein said alkyl portion is optionally substituted with one to three fluoros, or said alkyl portion is substituted with R′R″N— or R′R″NCH₂— wherein R′ and R″ are independently H or C1-C6 alkyl. In one embodiment, hetCyc¹ is a 6-membered heterocyclic ring having 1-2 ring nitrogen atoms, wherein the heterocyclic ring is optionally substituted with cyclopropyl. Non-limiting examples include the structures:

In one embodiment, D is hetCyc¹ and E is (hydroxy C1-C6 alkyl)C(═O)— optionally substituted with one to three fluoros. In one embodiment, hetCyc¹ is a 6-membered heterocyclic ring having two ring nitrogen atoms, wherein the heterocyclic ring is optionally substituted with cyclopropyl. Non-limiting examples include the structures:

In one embodiment, D is hetCyc¹ and E is (C1-C6 alkoxy)C(═O)—. In one embodiment, hetCyc¹ is a 6-membered heterocyclic ring having 1-2 ring nitrogen atoms, wherein the heterocyclic ring is optionally substituted with cyclopropyl or C1-C3 alkyl. Non-limiting examples include the structures:

In one embodiment, D is hetCyc¹ and E is (C1-C6 alkoxy)(C1-C6 alkyl)C(═O)—. In one embodiment, hetCyc¹ is a 6-membered heterocyclic ring having two ring nitrogen atoms. Non-limiting examples include the structures:

In one embodiment, D is hetCyc¹ and E is HC(═O)—. In one embodiment, hetCyc¹ is a 6-membered heterocyclic ring having one ring nitrogen atom. A non-limiting example is the structure:

In one embodiment, D is hetCyc¹ and E is Cyc¹, where Cyc¹ is a C3-C6 cycloalkyl, wherein the cycloalkyl is optionally substituted with one or more substituents independently selected from the group consisting of OH, halogen, C1-C6 alkoxy, CN, hydroxyC1-C6 alkyl-, (C1-C6 alkoxy)C1-C6 alkyl-, and C1-C6 alkyl optionally substituted with 1-3 fluoros. In one embodiment, Cyc¹ is a C3-C6 cycloalkyl optionally substituted with OH. In one embodiment, hetCyc¹ is a 6-membered heterocyclic ring having two ring nitrogen atoms. Non-limiting examples when D is hetCyc¹ and E is Cyc¹ include the structures:

In one embodiment, D is hetCyc¹ and E is Cyc¹C(═O)— where Cyc¹ is as defined for Formula I. In one embodiment, Cyc¹ is a C3-C6 cycloalkyl, wherein the cycloalkyl is optionally substituted with one or more substituents independently selected from the group consisting of OH, halogen, CN, hydroxyC1-C6 alkyl-, (C1-C6 alkoxy)C1-C6 alkyl- or C1-C6 alkyl optionally substituted with 1-3 fluoros, or the cycloalkyl is substituted with phenyl, wherein the phenyl is optionally substituted with one or more substituents independently selected from the group consisting of halogen, C1-C3 alkyl, C1-C3 alkoxy and CF₃ or the cycloalkyl is substituted with a 5-6 membered heteroaryl ring having 1-3 ring heteroatoms independently selected from N and O, wherein the heteroaryl ring is optionally substituted with one or more substituents independently selected from the group consisting of halogen, C1-C3 alkyl, C1-C3 alkoxy and CF₃. In one embodiment, the cycloalkyl is substituted with phenyl. In one embodiment, hetCyc¹ is a 6-membered heterocyclic ring having two ring nitrogen atoms. Non-limiting examples when D is hetCyc¹ and E is Cyc¹C(═O)— include the structures:

In one embodiment, D is hetCyc¹ and E is Cyc¹(C1-C6 alkyl)C(═O)— wherein the alkyl portion is optionally substituted with one or more groups independently selected from the group consisting of OH, fluoro, C1-C3 alkoxy, and R^(c)R^(d)N— where R^(c) and R^(d) are independently H or C1-C6 alkyl. In one embodiment, Cyc¹ is a C3-C6 cycloalkyl optionally substituted with one or more substituents independently selected from the group consisting of OH, halogen, C1-C6 alkoxy, CN, hydroxyC1-C6 alkyl-, (C1-C6 alkoxy)C1-C6 alkyl-, and C1-C6 alkyl optionally substituted with 1-3 fluoros. In one embodiment, the alkyl portion of Cyc¹(C1-C6 alkyl)C(═O)— is unsubstituted. In one embodiment, Cyc¹ is unsubstituted. In one embodiment, hetCyc¹ is a 6-membered heterocyclic ring having two ring nitrogen atoms. A non-limiting example when D is hetCyc¹ and E is Cyc¹(C1-C6 alkyl)C(═O)— is the structure:

In one embodiment, D is hetCyc¹ and E is hetCyc⁴, where hetCyc⁴ is as defined for Formula I. In one embodiment, hetCyc⁴ is a 4-6 membered heterocyclic ring having a ring heteroatom selected from O and S wherein the S is optionally oxidized to SO₂, and wherein the heterocyclic ring is optionally substituted with OH or C1-C6 alkoxy. In one embodiment, hetCyc¹ is a 6-membered heterocyclic ring having two ring nitrogen atoms. Non-limiting examples when D is hetCyc¹ and E is hetCyc⁴ include the structures:

In one embodiment, D is hetCyc¹ and E is hetCyc⁴C(═O)—, where hetCyc⁴ is as defined for Formula I. In one embodiment, hetCyc⁴ is optionally substituted with one or more substituents independently selected from the group consisting of halogen, OH, CN, C1-C6 alkyl (optionally substituted with 1-3 fluoros), C1-C6 alkoxy, (C1-C6 alkoxy)C1-C6 alkyl-, (C3-C6)cycloalkyl, a 5-6 membered heterocyclic ring having 1-2 ring heteroatoms independently selected from N and O, and phenyl wherein said phenyl is optionally substituted with one or more substituents independently selected from the group consisting of halogen, C1-C6 alkyl and C1-C6 alkoxy. In one embodiment, the ring is optionally substituted with one or more substituents independently selected from the group consisting of halogen, OH, CN, C1-C6 alkyl (optionally substituted with 1-3 fluoros), C1-C6 alkoxy and (C1-C6 alkoxy)C1-C6 alkyl-. In one embodiment, hetCyc¹ is a 6-membered heterocyclic ring having two ring nitrogen atoms. Non-limiting examples when D is hetCyc¹ and E is hetCyc⁴C(═O)— include the structures:

In one embodiment, D is hetCyc¹ and E is hetCyc⁴(C1-C6 alkyl)C(═O)— where hetCyc⁴ is as defined for Formula I. In one embodiment, hetCyc⁴ is a 5-6 membered heterocyclic ring having 1-2 ring heteroatoms independently selected from N and O, wherein the heterocyclic ring is optionally substituted with C1-C6 alkyl. In one embodiment, hetCyc¹ is a 6-membered heterocyclic ring having two ring nitrogen atoms. Non-limiting examples when D is hetCyc¹ and E is hetCyc⁴(C1-C6 alkyl)C(═O)— include the structures:

In one embodiment, D is hetCyc¹ and E is hetCyc⁴C(═O)C1-C6 alkyl-, where hetCyc⁴ is as defined for Formula I. In one embodiment, hetCyc⁴ is a 4-6 membered heterocyclic ring having 1-2 ring heteroatoms independently selected from N and O. In one embodiment, hetCyc⁴ is unsubstituted. In one embodiment, hetCyc¹ is a 6-membered heterocyclic ring having two ring nitrogen atoms. A non-limiting example when D is hetCyc¹ and E is hetCyc⁴C(═O)C1-C6 alkyl- is the structure:

In one embodiment, D is hetCyc¹ and E is hetCyc⁴C(═O)NR^(g)—, where R^(g) is H or C1-C6 alkyl, where hetCyc⁴ is as defined for Formula I. In one embodiment, hetCyc⁴ is optionally substituted with one or more substituents independently selected from the group consisting of halogen, OH, CN, C1-C6 alkyl (optionally substituted with 1-3 fluoros), C1-C6 alkoxy, and (C1-C6 alkoxy)C1-C6 alkyl-. In one embodiment, hetCyc¹ is a 6-membered heterocyclic ring having two ring nitrogen atoms

Non-limiting examples when D is hetCyc¹ and E is hetCyc⁴C(═O)NR^(g)—, where R^(g) is H or C1-C6 alkyl include the structures:

In one embodiment, D is hetCyc¹ and E is Ar² wherein Ar² is as defined for Formula I. In one embodiment, Ar² is phenyl optionally substituted with one or more substituents independently selected from the group consisting of halogen. In one embodiment, hetCyc¹ is a 4-6 membered heterocyclic ring having 1-2 ring atoms independently selected from N and O. Non-limiting examples when D is hetCyc¹ and E is Ar² include the structures:

In one embodiment, D is hetCyc¹ and E is Ar²C(═O)— wherein Ar² is as defined for Formula I. In one embodiment, Ar² is phenyl optionally substituted with one or more substituents independently selected from the group consisting of halogen or a 5-6 membered heterocyclic ring having 1-2 ring heteroatoms independently selected from N and O. In one embodiment, hetCyc¹ is a 6-membered ring having two ring nitrogen atoms. Non-limiting examples include the structures:

In one embodiment, D is hetCyc¹ and E is (Ar²)C1-C6 alkyl- wherein Ar² is as defined for Formula I. In one embodiment, Ar² is phenyl optionally substituted with one or more substituents independently selected from the group consisting of halogen, C1-C3 alkyl, C1-C3 alkoxy, CN, and R^(i)R^(j)N— where R^(i) and R^(j) are independently selected from H and C1-C6 alkyl. In one embodiment, Ar² is phenyl optionally substituted with one or more substituents independently selected from the group consisting of halogen, C1-C6 alkyl, C1-C6 alkoxy, CN, and R^(i)R^(j)N— where R^(i) and R^(j) are independently selected from H and C1-C6 alkyl. In one embodiment, hetCyc¹ is a 4-6-membered ring having one or two ring nitrogen atoms wherein said ring is optionally substituted with oxo or OH. Non-limiting examples when D is hetCyc¹ and E is (Ar²)C1-C6 alkyl- include the structures:

In one embodiment, D is hetCyc¹ and E is (Ar²)hydroxy C2-C6 alkyl- wherein Ar² is as defined for Formula I. In one embodiment, Ar² is phenyl optionally substituted with one or more halogens. In one embodiment, hetCyc¹ is a 6-membered ring having two ring nitrogen atoms. Non-limiting examples when D is hetCyc¹ and E is (Ar²)hydroxy C2-C6 alkyl- include the structures:

In one embodiment, D is hetCyc¹ and E is Ar²(C1-C6 alkyl)C(═O)—, wherein Ar² is as defined for Formula I and the alkyl portion is optionally substituted with one or two groups independently selected from the group consisting of OH, C1-C6 alkyl (optionally substituted with 1-3 fluoros), hydroxyC1-C6 alkyl-, (C1-C6)alkoxy, R^(e)R^(f)N— and (R^(e)R^(f)N)C1-C3 alkyl- wherein R^(e) and R^(f) are independently H or C1-C6 alkyl, or said alkyl portion is substituted with a 5-6 membered heterocyclic ring having one or two ring heteroatoms independently selected from N and O, wherein the heterocyclic ring is optionally substituted with C1-C6 alkyl. In one embodiment, hetCyc¹ is piperazinyl. In one embodiment, Ar² is phenyl optionally substituted with one or more substituents independently selected from halogen, CN, C1-C6 alkyl and C1-C6 alkoxy (optionally substituted with 1-3 fluoros).

In one embodiment, D is hetCyc¹ and E is Ar²(C1-C6 alkyl)C(═O)—, wherein Ar² is as defined for Formula I and the alkyl portion is optionally substituted with one or two groups independently selected from the group consisting of OH, C1-C6 alkyl, hydroxyC1-C6 alkyl-, (C1-C6)alkoxy, R^(e)R^(f)N— and (R^(e)R^(f)N)C1-C3 alkyl- wherein R^(e) and R^(f) are independently H or C1-C6 alkyl. In one embodiment, hetCyc¹ is a 6-membered ring having two ring nitrogen atoms. Non-limiting examples when D is hetCyc¹ and E is Ar²(C1-C6 alkyl)C(═O)— include the structures:

In one embodiment, D is hetCyc¹ and E is hetAr²C(═O)—, where hetAr² is as defined for Formula I. In one embodiment, hetAr² is optionally substituted with one or more substituents independently selected from the group consisting of C1-C3 alkyl, (C3-C6)cycloalkyl and (C1-C6 alkoxy)C1-C6 alkyl-. In one embodiment, hetCyc¹ is a 6-membered ring having two ring nitrogen atoms. Non-limiting examples when D is hetCyc¹ and E is hetAr²C(═O)— include the structures:

In one embodiment, D is hetCyc¹ and E is (hetAr²)hydroxy C2-C6 alkyl- where hetAr² is as defined for Formula I. In one embodiment, hetAr² is a 5-6 membered heteroaryl ring having 1-2 ring heteroatoms independently selected from N and O wherein said ring is unsubstituted. In one embodiment, hetCyc¹ is a 6-membered ring having two ring nitrogen atoms. Non-limiting examples includes the structures:

In one embodiment, D is hetCyc¹ and E is hetAr²(C1-C6 alkyl)C(═O)—, wherein hetAr² is as defined for Formula I and the alkyl portion is optionally substituted with one or two groups independently selected from the group consisting of OH, C1-C6 alkyl, hydroxyC1-C6 alkyl-, (C1-C6)alkoxy, R^(e)R^(f)N— and (R^(e)R^(f)N)C1-C3 alkyl-, where R^(e) and R^(f) are independently H or C1-C6 alkyl. In one embodiment, the alkyl portion of hetAr²(C1-C6 alkyl)C(═O)— is unsubstituted. In one embodiment, hetAr² is optionally substituted with one or more substituents independently selected from the group consisting of halogen and C1-C6 alkyl. In one embodiment, hetCyc¹ is a 6-membered ring having two ring nitrogen atoms. Non-limiting examples where D is hetCyc¹ and E is hetAr²(C1-C6 alkyl)C(═O)— include the structures:

In one embodiment, D is hetCyc¹ and E is R¹R²NC(═O)—, where R′ is H, C1-C6 alkyl or (C1-C6 alkoxy)C1-C6 alkyl-, and R² is C1-C6 alkyl (optionally substituted with 1-3 fluoros), (C1-C6 alkoxy)C1-C6 alkyl- (optionally substituted with 1-3 fluoros), Cyc³, hydroxyC1-C6 alkyl- (optionally substituted with 1-3 fluoros), C1-C6 alkoxy (optionally substituted with 1-3 fluoros), hetCyc⁷, Ar³, Ar³CH₂—, hydroxyC1-C6 alkoxy or (C3-C6 cycloalkyl)CH₂O—. In one embodiment, hetCyc¹ is optionally substituted with C1-C3 alkyl. Non-limiting examples when D is hetCyc¹ and E is R¹R²NC(═O)— include the structures:

In one embodiment, D is hetCyc¹ and E is R¹R²N(C1-C6 alkyl)C(═O)— wherein the C1-C3 alkyl portion is optionally substituted with phenyl. In one embodiment, R¹ is H or C1-C6 alkyl and R² is H, C1-C6 alkyl (optionally substituted with 1-3 fluoros) or (C1-C6 alkoxy)C(═O)—. In one embodiment, hetCyc¹ is a 6-membered ring having two ring nitrogen atoms. Non-limiting examples include the structures:

In one embodiment, D is hetCyc¹ and E is R¹R²NC(═O)C1-C6 alkyl-. In one embodiment, R¹ is H or C1-C6 alkyl and R² is C1-C6 alkyl (optionally substituted with 1-3 fluoros). In one embodiment, hetCyc¹ is a 4-6-membered ring having one to two ring nitrogen atoms. Non-limiting examples include the structures:

In one embodiment, D is hetCyc¹ and E is R¹R²NC(═O)NH—, where R¹ is H or C1-C6 alkyl, and R² is C1-C6 alkyl (optionally substituted with 1-3 fluoros). In one embodiment, hetCyc¹ is a 6-membered ring having one ring nitrogen atom. Non-limiting examples include the structures:

In one embodiment, D is hetCyc¹ and E is CH₃SO₂(C1-C6 alkyl)C(═O)—. In one embodiment, hetCyc¹ is a 6-membered ring having two ring nitrogen atoms. A non-limiting example is the structure:

In one embodiment, D is hetCyc¹ and E is (C1-C6 alkyl)SO₂—. In one embodiment, hetCyc¹ is a 6-membered ring having one or two ring nitrogen atoms. Non-limiting examples include the structures:

In one embodiment, D is hetCyc¹ and E is (C3-C6 cycloalkyl)CH₂SO₂—. In one embodiment, hetCyc¹ is a 6-membered ring having two ring nitrogen atoms. A non-limiting example is the structure:

In one embodiment, D is hetCyc¹ and E is hetCyc⁵-SO₂—, where hetCyc⁵ is a 5-6 membered heterocyclic ring having a ring heteroatom selected from O and N. In one embodiment, hetCyc¹ is a 6-membered ring having two ring nitrogen atoms. Non-limiting examples include the structures:

In one embodiment, D is hetCyc¹ and E is R⁴R⁶NSO₂—, where R⁴ and R⁵ are independently H or C1-C6 alkyl. In one embodiment, hetCyc¹ is a 6-membered ring having one or two ring nitrogen atoms. Non-limiting examples include the structures:

In one embodiment, D is hetCyc¹ and E is R⁶C(═O)NH—, where R⁶ is C1-C6 alkyl, hydroxyC1-C6 alkyl-, C1-C6 alkoxy, (C1-C6 alkoxy)C1-C6 alkyl-, phenyl or hetCyc⁸. In one embodiment, hetCyc¹ is a 6-membered ring having one ring nitrogen atom. Non-limiting examples include the structures:

In one embodiment, D is hetCyc¹ and E is hetCyc⁶, where hetCyc⁶ is a 5 membered heterocyclic ring having one or two ring heteroatoms independently selected from N and O, wherein the ring is substituted with oxo and wherein the ring is further optionally substituted with one or more substituents independently selected from the group consisting of OH and C1-6 alkyl. In one embodiment, hetCyc¹ is a 6-membered ring having one or two ring nitrogen atoms. Non-limiting examples include the structures:

In one embodiment, D is hetCyc¹ and E is (hetAr²)C1-C6 alkyl-, where hetAr² is as defined for Formula I. In one embodiment, hetAr² is optionally substituted with one or more substituents independently selected from the group consisting of halogen, C1-C3 alkyl and C1-C3 alkoxy. In one embodiment, hetCyc¹ is a 6-membered ring having one or two ring nitrogen atoms, wherein said ring is optionally substituted with OH. Non-limiting examples when D is hetCyc¹ and E is (hetAr²)C1-C6 alkyl-include the structures:

In one embodiment, D is hetCyc¹ and E is (hetCyc⁴)C1-C6 alkyl-, where hetCyc⁴ is as defined for Formula I. In one embodiment, hetCyc⁴ is a 4-6 membered heterocyclic ring having 1-2 ring heteroatoms independently selected from N and O, wherein said heterocyclic ring is optionally substituted with (C1-C6 alkyl)C(═O)—. In one embodiment, hetCyc¹ is a 6-membered ring having one or two ring nitrogen atoms. Non-limiting embodiments when D is hetCyc¹ and E is (hetCyc⁴)C1-C6 alkyl-include the structures:

In one embodiment, D is hetCyc¹ and E is (C1-C6 alkoxy)C1-C6 alkyl- wherein said alkoxy portion is optionally substituted with 1-3 fluoros. In one embodiment, hetCyc¹ is a 6-membered ring having two ring nitrogen atoms. Non-limiting examples include the structures:

In one embodiment, D is hetCyc¹ and E is (C3-C6 cycloalkoxy)C1-C6 alkyl-. In one embodiment, hetCyc¹ is a 6-membered ring having two ring nitrogen atoms. A non-limiting example is the structure:

In one embodiment, D is hetCyc¹ and E is (C3-C6 cycloalkyl)C1-C6 alkyl- wherein said cycloalkyl is optionally substituted with 1-2 fluoros. In one embodiment, hetCyc¹ is a 6-membered ring having two ring nitrogen atoms. Non-limiting examples include the structures:

In one embodiment, D is hetCyc¹ and E is (R^(g)R^(h)N)C1-C6 alkyl- wherein R^(g) and R^(h) are independently H or C1-C6 alkyl. In one embodiment, hetCyc¹ is a 6-membered ring having one or two ring nitrogen atoms. Non-limiting examples include the structures:

In one embodiment, D is hetCyc¹ and E is Ar²—O—, where Ar² is as defined for Formula I. In one embodiment, Ar² is phenyl optionally substituted with one or more groups independently selected from halogen and CN. In one embodiment, hetCyc¹ is a 6-membered ring having one ring nitrogen atom. Non-limiting examples include the structures:

In one embodiment, D is hetCyc¹ and E is (C1-C6 alkyl)SO₂C1-C6 alkyl-. In one embodiment, hetCyc¹ is a 6-membered ring having two ring nitrogen atoms. A non-limiting example is the structure:

In one embodiment, D is hetCyc¹ and E is (C1-C6 alkoxy)C(═O)NHC1-C6 alkyl-. In one embodiment, hetCyc¹ is a 6-membered ring having two ring nitrogen atoms. A non-limiting example is the structure:

In one embodiment, D is hetCyc¹ and E is (C3-C6 cycloalkyl)SO₂— wherein said cycloalkyl is optionally substituted with C1-C6 alkyl. In one embodiment, hetCyc¹ is a 6-membered ring having two ring nitrogen atoms. A non-limiting example includes the structure:

In one embodiment, D is hetCyc¹ and E is (N—(C1-C3 alkyl)pyridinonyl)C1-C6 alkyl-. In one embodiment, hetCyc¹ is a 6-membered ring having two ring nitrogen atoms. Non-limiting examples include the structures:

In one embodiment, D is hetCyc¹ and E is (Ar⁴SO₂)C1-C6 alkyl-, where Ar⁴ is as defined for Formula I. In one embodiment, hetCyc¹ is a 6-membered ring having two ring nitrogen atoms. A non-limiting example includes the structure:

In one embodiment, D is hetCyc¹ and E is (hetAr²)—O—, where hetAr² is as defined for Formula I. In one embodiment, hetAr² is optionally substituted with one or more substituents independently selected from C1-C6 alkyl and C1-C6 alkoxy. In one embodiment, hetCyc¹ is a 6-membered ring having two ring nitrogen atoms. Non-limiting examples include the structures:

In one embodiment of Formula I, D is hetCyc², where hetCyc² is a 7-8 membered bridged heterocyclic ring having 1-3 ring heteroatoms independently selected from N and O, wherein the heterocyclic ring is optionally substituted with one or more substituents independently selected from the group consisting of C1-C3 alkyl. In one embodiment, hetCyc² is a 7-8 membered bridged heterocyclic ring having 1-2 ring nitrogen atoms, wherein the ring is optionally substituted with one or more substituents independently selected from the group consisting of C1-C3 alkyl. In one embodiment, hetCyc² is unsubstituted. Non-limiting examples of D when represented by hetCyc² include the structures:

where the asterisk indicates the point of attachment to the E group and the wavy line indicates the point of attachment to the ring comprising X¹, X², X³ and X⁴, wherein X¹, X², X³, X⁴ and E are as defined for Formula I.

In one embodiment, hetCyc² is:

where the asterisk indicates the point of attachment to the E group and the wavy line indicates the point of attachment to the ring comprising X¹, X², X³ and X⁴, wherein X¹, X², X³, X⁴ and E are as defined for Formula I.

In one embodiment of Formula I, D is hetCyc² and E is (a) hydrogen, (b) OH, (c) R′R″N(CH₂)_(n)—, wherein R′ is H or C1-C6 alkyl, R″ is H, C1-C6 alkyl or phenyl, and n is 0 or 1, (d) C1-C6 alkyl optionally substituted with one to three fluoros, (e) hydroxyC1-C6 alkyl- optionally substituted with one to three fluoros, (f) C1-C6 alkoxy optionally substituted with one to three fluoros, (i) (C1-C6 alkyl)C(═O)— optionally substituted with one to three fluoros, (k) (C1-C6 alkoxy)C(═O)—, (o) Cyc¹C(═O)—, (x) (Ar²)C1-C6 alkyl-, (y) (Ar²)hydroxy C2-C6 alkyl-, (ee) R¹R²N(C1-C6 alkyl)C(═O)— wherein said alkyl portion is optionally substituted with phenyl, (mm) R⁶C(═O)NH—, or (oo) hetAr²C1-C6 alkyl-, where Cyc¹, Ar², R¹, R², hetAr² and R⁶ are as defined for Formula I.

In one embodiment of Formula I, D is hetCyc² and E is (a) hydrogen, (c) R′R″N(CH₂)_(n)— wherein R′ is H or C1-C6 alkyl, R″ is H, C1-C6 alkyl or phenyl, and n is 0 or 1, (mm) R⁶C(═O)NH—, or (oo) hetAr²C1-C6 alkyl-, where R⁶ and hetAr² are as defined for Formula I.

In one embodiment, D is hetCyc² and E is hydrogen. In one embodiment, hetCyc² is a 7-8 membered bridged heterocyclic ring having 1-2 ring nitrogen atoms. Non-limiting examples include the structures:

In one embodiment, D is hetCyc² and E is OH. In one embodiment, hetCyc² is a 7-8 membered bridged heterocyclic ring having one ring nitrogen atom. A non-limiting example is the structure:

In one embodiment, D is hetCyc² and E is R′R″N(CH₂)_(n)—, wherein R′ is H or C1-C6 alkyl, R″ is H, C1-C6 alkyl or phenyl, and n is 0 or 1. In one embodiment, hetCyc² is a 7-8 membered bridged heterocyclic ring having one ring nitrogen atom. Non-limiting examples include the structures:

In one embodiment, D is hetCyc² and E is C1-C6 alkoxy optionally substituted with one to three fluoros. In one embodiment, hetCyc² is a 7-8 membered bridged heterocyclic ring having one ring nitrogen atom. A non-limiting example is the structure:

In one embodiment, D is hetCyc² and E is (C1-C6 alkyl)C(═O)— optionally substituted with one to three fluoros. In one embodiment, hetCyc² is a 7-8 membered bridged heterocyclic ring having two ring nitrogen atoms. Non-limiting examples include the structures:

In one embodiment, D is hetCyc² and E is (C1-C6 alkoxy)C(═O)—. In one embodiment, hetCyc² is a 7-8 membered bridged heterocyclic ring having two ring nitrogen atoms. Non-limiting examples include the structures:

In one embodiment, D is hetCyc² and E is (Ar²)C1-C6 alkyl where Ar² is as defined for Formula I. In one embodiment, Ar² is an unsubstituted phenyl. In one embodiment, hetCyc² is a 7-8 membered bridged heterocyclic ring having two ring nitrogen atoms. Non-limiting examples when D is hetCyc² and E is (Ar²)C1-C6 alkyl include the structures:

In one embodiment, D is hetCyc² and E is R¹R²N(C1-C6 alkyl)C(═O)—. In one embodiment, hetCyc² is a 7-8 membered bridged heterocyclic ring having two ring nitrogen atoms. A non-limiting example is the structure:

In one embodiment, D is hetCyc² and E is R⁶C(═O)NH—, where R⁶ is as defined for Formula I. In one embodiment, hetCyc² is a 7-8 membered bridged heterocyclic ring having two ring nitrogen atoms. A non-limiting example is the structure:

In one embodiment, D is hetCyc² and E is hetAr²C1-C6 alkyl-, where hetAr² is as defined for Formula I. In one embodiment, hetCyc² is a 7-8 membered bridged heterocyclic ring having two ring nitrogen atoms. A non-limiting example is the structure:

In one embodiment of Formula I, D is hetCyc³, where hetCyc³ is a 7-11 membered heterospirocyclic ring having 1-2 ring heteroatoms independently selected from N and O and wherein the ring is optionally substituted with C1-C3 alkyl. In one embodiment, hetCyc³ is unsubstituted. Non-limiting examples when D is represented by hetCyc³ include the structures:

where the asterisk indicates the point of attachment to the E group and the wavy line indicates the point of attachment to the ring comprising X¹, X², X³ and X⁴, wherein X¹, X², X³, X⁴ and E are as defined for Formula I.

In one embodiment, D is hetCyc³ and E is selected from (a) hydrogen, (c) R′R″N(CH₂)_(n)— wherein R′ is H or C1-C6 alkyl, R″ is H, C1-C6 alkyl or phenyl, and n is 0 or 1, (d) C1-C6 alkyl optionally substituted with one to three fluoros, (e) hydroxyC1-C6 alkyl optionally substituted with one to three fluoros, (i) (C1-C6 alkyl)C(═O)— optionally substituted with one to three fluoros, (j) (hydroxy C1-C6 alkyl)C(═O)— optionally substituted with one to three fluoros, (k) (C1-C6 alkoxy)C(═O)—, (o) Cyc¹C(═O)—, (p) Cyc¹(C1-C6 alkyl)C(═O), (r) hetCyc⁴C(═O)—, (w) Ar²C(═O)—, (x) (Ar²)C1-C6 alkyl-, (y) (Ar²)hydroxy C2-C6 alkyl-, (z) Ar²(C1-C6 alkyl)C(═O)— wherein said alkyl portion is optionally substituted with one or two groups independently selected from the group consisting of OH, C1-C6 alkyl (optionally substituted with 1-3 fluoros), hydroxyC1-C6 alkyl-, (C1-C6)alkoxy, R^(e)R^(f)N— and (R^(e)R^(f)N)C1-C3 alkyl- where R^(e) and R^(f) are independently H or C1-C6 alkyl, or said alkyl portion is substituted with a 5-6 membered heterocyclic ring having one or two ring heteroatoms independently selected from N and O and wherein the heterocyclic ring is optionally substituted with C1-C6 alkyl, (dd) R¹R²NC(═O)—, (ee) R¹R²N(C1-C6 alkyl)C(═O)—, (mm) R⁶C(═O)NH—, (xx) (C3-C6 cycloalkoxy)C(═O)— and (zz) Ar⁴CH₂OC(═O)—.

In one embodiment, D is hetCyc³ and E is hydrogen. Non-limiting examples include the structures:

In one embodiment, D is hetCyc³ and E is R′R″N(CH₂)_(n)—, wherein R′ is H or C1-C6 alkyl, R″ is H, C1-C6 alkyl or phenyl, and n is 0 or 1. In one embodiment, R′ and R″ are H. A non-limiting example is the structure:

In one embodiment, D is hetCyc³ and E is C1-C6 alkyl optionally substituted with one to three fluoros. Non-limiting examples include the structures:

In one embodiment, D is hetCyc³ and E is hydroxyC1-C6 alkyl- optionally substituted with one to three fluoros. Non-limiting examples include the structures:

In one embodiment, D is hetCyc³ and E is (C1-C6 alkyl)C(═O)— optionally substituted with one to three fluoros. Non-limiting examples include the structures:

In one embodiment, D is hetCyc³ and E is (hydroxy C1-C6 alkyl)C(═O)— optionally substituted with one to three fluoros. Non-limiting examples include the structures:

In one embodiment, D is hetCyc³ and E is (C1-C6 alkoxy)C(═O)—. Non-limiting examples include the structures:

In one embodiment, D is hetCyc³ and E is Cyc¹C(═O)—, where Cyc¹ is as defined for Formula I. In one embodiment, Cyc¹ is unsubstituted. Non-limiting examples include the structures:

In one embodiment, D is hetCyc³ and E is Cyc¹(C1-C6 alkyl)C(═O)— wherein said alkyl portion is optionally substituted with one or more groups independently selected from the group consisting of OH, fluoro, C1-C3 alkoxy and R^(c)R^(d)N—, where R^(c) and R^(d) are independently H or C1-C6 alkyl, and Cyc¹ is as defined for Formula I.

In one embodiment, D is hetCyc³ and E is Cyc¹(C1-C6 alkyl)C(═O)— wherein said alkyl portion is unsubstituted, and Cyc¹ is as defined for Formula I. In one embodiment, Cyc¹ is an unsubstituted C3-C6 cycloalkyl.

Non-limiting examples when D is hetCyc³ and E is Cyc¹(C1-C6 alkyl)C(═O)— include the structures:

In one embodiment, D is hetCyc³ and E is hetCyc⁴C(═O)—, where hetCyc⁴ is as defined for Formula I. In one embodiment, hetCyc⁴ is a 4-6 membered heterocyclic ring having 1-2 ring heteroatoms independently selected from N and O, wherein said ring is unsubstituted. A non-limiting example when D is hetCyc³ and E is hetCyc⁴C(═O)— is the structure:

In one embodiment, D is hetCyc³ and E is Ar²C(═O)— where Ar² is as defined for Formula I. In one embodiment, Ar² is unsubstituted. A non-limiting example is the structure:

In one embodiment, D is hetCyc³ and E is (Ar²)C1-C6 alkyl-. In one embodiment, Ar² is phenyl which is unsubstituted. Non-limiting examples include the structures:

In one embodiment, D is hetCyc³ and E is Ar²(C1-C6 alkyl)C(═O)— wherein the alkyl portion is optionally substituted with one or two groups independently selected from the group consisting of OH, C1-C6 alkyl, hydroxyC1-C6 alkyl-, (C1-C6)alkoxy, R^(e)R^(f)N— and (R^(e)R^(f)N)C1-C3 alkyl-, where R^(e) and R^(f) are independently H or C1-C6 alkyl, or said alkyl portion is substituted with a 5-6 membered heterocyclic ring having one or two ring heteroatoms independently selected from N and O, wherein the heterocyclic ring is optionally substituted with C1-C6 alkyl, and Ar² is as defined for Formula I. In one embodiment, D is hetCyc³ and E is Ar²(C1-C6 alkyl)C(═O)— wherein the alkyl portion is unsubstituted. In one embodiment, Ar² is phenyl which is unsubstituted. A non-limiting example is the structure:

In one embodiment, D is hetCyc³ and E is R¹R²NC(═O)— where R¹ and R² are as defined for Formula I. In one embodiment, R¹ is H or C1-C6 alkyl and R² is H or C1-C6 alkyl optionally substituted with 1-3 fluoros. Non-limiting examples include the structures:

In one embodiment, D is hetCyc³ and E is R¹R²N(C1-C6 alkyl)C(═O)— wherein the C1-C3 alkyl portion is optionally substituted with phenyl, and R¹ and R² are as defined for Formula I. In one embodiment, R¹ is H or C1-C6 alkyl and R² is H or C1-C6 alkyl optionally substituted with 1-3 fluoros. A non-limiting example is the structure:

In one embodiment, D is hetCyc³ and E is R⁶C(═O)NH—, where R⁶ is C1-C6 alkyl, hydroxyC1-C6 alkyl-, C1-C6 alkoxy, (C1-C6 alkoxy)C1-C6 alkyl-, phenyl or hetCyc⁸. In one embodiment, R⁶ is C1-C6 alkoxy. A non-limiting example is the structure:

In one embodiment, D is hetCyc³ and E is (C3-C6 cycloalkoxy)C(═O)—. A non-limiting example is the structure:

In one embodiment, D is hetCyc³ and E is Ar⁴CH₂OC(═O)—. A non-limiting example is the structure:

In one embodiment, Formula I includes compounds of Formula I-A, wherein:

X¹ is CH or N, and each of X², X³ and X⁴ is CH;

A is H, Cl or CN;

B is hetAr¹;

hetAr¹ is pyrazolyl optionally substituted with one or more substituents independently selected from the group consisting of C1-C6 alkyl (optionally substituted with one to three fluoros), (C1-C6 alkoxy)C1-C6 alkyl-, (C1-C6 alkylSO₂)C1-C6 alkyl-, hetCyc^(a), and hetCyc^(a)C1-C6 alkyl;

hetCyc^(a) is a 4-6 membered heterocyclic ring having a ring heteroatom selected from N and O, wherein the heterocyclic ring is optionally substituted with halogen, C1-C6 alkyl (optionally substituted with one to three fluoros), (C1-C6 alkoxy)C1-C6 alkyl-, di(C1-C3 alkyl)NCH₂C(═O)—, (C1-C6 alkoxy)C(═O)— or (C1-C6 alkoxy)CH₂C(═O)—;

D is hetCyc¹ or hetCyc²;

hetCyc¹ is a 4-6 membered heterocyclic ring having 1-2 ring heteroatoms independently selected from N and O, wherein the heterocyclic ring is optionally substituted with one or more substituents independently selected from the group consisting of C1-C3 alkyl (optionally substituted with one to three fluoros), or said heterocyclic ring is substituted with a cycloalkylidene ring, or said heterocyclic ring is substituted with an oxo group;

hetCyc² is a 7-8 membered bridged heterocyclic ring having 1-3 ring heteroatoms independently selected from N and O, wherein the heterocyclic ring is optionally substituted with one or more substituents independently selected from the group consisting of C1-C3 alkyl;

E is

(a) hydrogen,

(b) OH,

(c) R′R″N(CH₂)_(n)— wherein R′ is H or C1-C6 alkyl, R″ is H, C1-C6 alkyl or phenyl, and n is 0 or 1,

(d) C1-C6 alkyl optionally substituted with one to three fluoros, hydroxyC1-C6 alkyl,

(f) C1-C6 alkoxy optionally substituted with one to three fluoros,

(g) hydroxyC1-C6 alkoxy- optionally substituted with one to three fluoros,

(h) (C1-C6 alkoxy)hydroxy C1-C6 alkyl- optionally substituted with one to three fluoros,

(j) (hydroxy C1-C6 alkyl)C(═O)— optionally substituted with one to three fluoros,

(k) (C1-C6 alkoxy)C(═O)—,

(l) (C1-C6 alkoxy)(C1-C6 alkyl)C(═O)—,

(m) HC(═O)—,

(n) Cyc¹,

(o) Cyc¹C(═O)—,

(p) Cyc¹(C1-C6 alkyl)C(═O)— wherein the alkyl portion is optionally substituted with one or more groups independently selected from the group consisting of OH, fluoro, C1-C3 alkoxy and R^(c)R^(d)N—, where R^(c) and R^(d) are independently H or C1-C6 alkyl,

(q) hetCyc⁴,

(r) hetCyc⁴C(═O)—,

(s) hetCyc⁴(C1-C6 alkyl)C(═O)—,

(t) hetCyc⁴C(═O)C1-C6 alkyl-,

(u) hetCyc⁴C(═O)NR^(g)—, where R^(g) is H or C1-C6 alkyl,

(v) Ar²,

(w) Ar²C(═O)—,

(x) (Ar²)C1-C6 alkyl)-,

(y) (Ar²)hydroxy C2-C6 alkyl-,

(z) Ar²(C1-C6 alkyl)C(═O)— wherein the alkyl portion is optionally substituted with one or two groups independently selected from the group consisting of OH, C1-C6 alkyl (optionally substituted with 1-3 fluoros), hydroxyC1-C6 alkyl, C1-C6 alkoxy, R^(e)R^(f)N— and (R^(e)R^(f)N)C1-C3 alkyl- wherein R^(e) and R^(f) are independently H or C1-C6 alkyl, or said alkyl portion is substituted with a 5-6 membered heterocyclic ring having one or two ring heteroatoms independently selected from N and O wherein the heterocyclic ring is optionally substituted with C1-C6 alkyl,

(aa) hetAr²C(═O)—,

(bb) (hetAr²)hydroxy C2-C6 alkyl-,

(cc) hetAr²(C1-C6 alkyl)C(═O)— wherein the alkyl portion is optionally substituted with one or two groups independently selected from the group consisting of OH, C1-C6 alkyl, hydroxyC1-C6 alkyl, C1-C6 alkoxy, R^(e)R^(f)N— and (R^(e)R^(f)N)C1-C3 alkyl-, wherein R^(e) and R^(f) are independently H or C1-C6 alkyl, or said alkyl portion is substituted with a 5-6 membered heterocyclic ring having one or two ring heteroatoms independently selected from N and O and wherein the heterocyclic ring is optionally substituted with C1-C6 alkyl,

(dd) R¹R²NC(═O)—,

(ee) R¹R²N(C1-C6 alkyl)C(═O)— wherein the alkyl portion is optionally substituted with phenyl,

(ff) R¹R²NC(═O)C1-C6 alkyl-,

(gg) R¹R²NC(═O)NH—,

(hh) CH₃SO₂(C1-C6 alkyl)C(═O)—,

(ii) (C1-C6 alkyl)SO₂—,

(jj) (C3-C6 cycloalkyl)CH₂SO₂—,

(kk) hetCyc⁵-SO₂—,

(ll) R⁴R⁵NSO₂—,

(mm) R⁶C(═O)NH—,

(nn) hetCyc⁶,

(oo) (hetAr²)C1-C6 alkyl-,

(pp) (hetCyc⁴)C1-C6 alkyl-,

(qq) (C1-C6 alkoxy)C1-C6 alkyl- wherein said alkoxy portion is optionally substituted with 1-3 fluoros,

(rr) (C3-C6 cycloalkoxy)C1-C6 alkyl-,

(ss) (C3-C6 cycloalkyl)C1-C6 alkyl- wherein said cycloalkyl is optionally substituted with 1-2 fluoros,

(tt) (R^(g)R^(h)N)C1-C6 alkyl- wherein R^(g) and R^(h) are independently H or C1-C6 alkyl,

(uu) Ar²—O—,

(vv) (C1-C6 alkyl)SO₂C1-C6 alkyl-,

(ww) (C1-C6 alkoxy)C(═O)NHC1-C6 alkyl-,

(yy) (C3-C6 cycloalkyl)SO₂— wherein said cycloalkyl is optionally substituted with C1-C6 alkyl,

(aaa) (N—(C1-C3 alkyl)pyridinonyl)C1-C6 alkyl-,

(bbb) (Ar⁴SO₂)C1-C6 alkyl- or

(ccc) hetAr²—O—;

Cyc¹ is a C3-C6 cycloalkyl, wherein (a) the cycloalkyl is optionally substituted with one or more substituents independently selected from the group consisting of OH, halogen, C1-C6 alkoxy, CN, hydroxyC1-C6 alkyl-, (C1-C6 alkoxy)C1-C6 alkyl-, and C1-C6 alkyl optionally substituted with 1-3 fluoros, or (b) the cycloalkyl is substituted with phenyl, wherein the phenyl is optionally substituted with one or more substituents independently selected from the group consisting of halogen, C1-C3 alkyl, C1-C3 alkoxy and CF₃, or (c) the cycloalkyl is substituted with a 5-6 membered heteroaryl ring having 1-3 ring heteroatoms independently selected from N and O, wherein the heteroaryl ring is optionally substituted with one or more substituents independently selected from the group consisting of halogen, C1-C3 alkyl, C1-C3 alkoxy and CF₃;

Ar² is phenyl optionally substituted with one or more substituents independently selected from the group consisting of halogen, C1-C6 alkyl (optionally substituted with one to three fluoros), C1-C6 alkoxy (optionally substituted with 1-3 fluoros), CN, a 5-6 membered heterocyclic ring having 1-2 ring heteroatoms independently selected from N and O, and R^(i)R^(j)N— where R^(i) and R^(j) are independently selected from H and C1-C6 alkyl;

hetAr² is a 5-6 membered monocyclic heteroaryl ring having 1-3 ring heteroatoms independently selected from N, O and S or a 9-10 membered bicyclic heteroaryl ring having 1-2 ring nitrogen atoms, wherein hetAr² is optionally substituted with one or more substituents independently selected from the group consisting of halogen, C1-C6 alkyl (optionally substituted with one to three fluoros), C1-C6 alkoxy (optionally substituted with 1-3 fluoros), hydroxyC1-C6 alkyl, (C3-C6)cycloalkyl, (C1-C6 alkoxy)C1-C6 alkyl-, CN and R′R″N— where R′ and R″ are independently H or C1-C3 alkyl;

hetCyc⁴ is (a) a 4-6 membered heterocyclic ring having 1-2 ring heteroatoms independently selected from N, O and S wherein said S is optionally oxidized to SO₂, (b) a 7-8 membered bridged heterocyclic ring having 1-2 ring heteroatoms independently selected from N and O, (c) a 6-12 membered fused bicyclic heterocyclic ring having 1-2 ring heteroatoms independently selected from N and O wherein the heterocyclic ring is optionally independently substituted with one to two C1-C6 alkyl substituents, or (d) a 7-10 membered spirocyclic heterocyclic ring having 1-2 ring heteroatoms independently selected from N and O, wherein each of the heterocyclic rings is optionally substituted with one or more substituents independently selected from the group consisting of halogen, OH, CN, C1-C6 alkyl (optionally substituted with 1-3 fluoros), C1-C6 alkoxy, (C1-C6 alkoxy)C1-C6 alkyl-, (C3-C6)cycloalkyl, (C1-C6 alkyl)C(═O)—, a 5-6 membered heterocyclic ring having 1-2 ring heteroatoms independently selected from N and O, and phenyl wherein said phenyl is optionally substituted with one or more substituents independently selected from halogen, C1-C6 alkyl and C1-C6 alkoxy;

R¹ is H, C1-C6 alkyl or (C1-C6 alkoxy)C1-C6 alkyl-;

R² is H, C1-C6 alkyl (optionally substituted with 1-3 fluoros), (C1-C6 alkoxy)C1-C6 alkyl-(optionally substituted with 1-3 fluoros), Cyc³, hydroxyC1-C6 alkyl (optionally substituted with 1-3 fluoros), C1-C6 alkoxy (optionally substituted with 1-3 fluoros), (C1-C6 alkoxy)C(═O), hetCyc⁷, Ar³, Ar³C1-C3 alkyl-, hydroxyC1-C6 alkoxy or (C3-C6 cycloalkyl)CH₂O—;

Cyc³ is a 3-6 membered carbocyclic ring optionally substituted with 1-2 groups independently selected from the group consisting of C1-C6 alkoxy, OH and halogen;

hetCyc⁷ is a 5-6 membered heterocyclic ring having a ring heteroatom selected from 0 and N wherein the ring is optionally substituted with C1-C6 alkyl;

Ar³ is phenyl optionally substituted with one or more substituents independently selected from halogen, C1-C3 alkyl (optionally substituted with one to three fluoros), and C1-C3 alkoxy;

R⁴ and R⁵ are independently H or C1-C6 alkyl;

R⁶ is C1-C6 alkyl, hydroxyC1-C6 alkyl, C1-C6 alkoxy, (C1-C6 alkoxy)C1-C6 alkyl-, phenyl or hetCyc⁸;

hetCyc⁸ is a 5-6 membered heterocyclic ring having a ring heteroatom selected from 0 and N, wherein the heterocyclic ring is optionally substituted with C1-C6 alkyl; and

Ar⁴ is phenyl optionally substituted with one or more halogens.

In one embodiment, Formula I includes compounds of Formula I-B, wherein:

X¹ is N and each of X², X³ and X⁴ is CH;

A is CN;

B is hetAr¹;

hetAr¹ is pyrazolyl optionally substituted with one or more substituents independently selected from C1-C6 alkyl (optionally substituted with one to three fluoros), (C1-C6 alkoxy)C1-C6 alkyl-, (C1-C6 alkylSO₂)C1-C6 alkyl-, hetCyc^(a), and hetCyc^(a)C1-C6 alkyl;

R^(a) and R^(b) are independently H or C1-C6 alkyl;

hetCyc^(a) is a 4-6 membered heterocyclic ring having a ring heteroatom selected from N and O, wherein the heterocyclic ring is optionally substituted with halogen, C1-C6 alkyl (optionally substituted with one to three fluoros), (C1-C6 alkoxy)C1-C6 alkyl-, di(C1-C3 alkyl)NCH₂C(═O)—, (C1-C6 alkoxy)C(═O)— or (C1-C6 alkoxy)CH₂C(═O)—;

D is hetCyc¹;

hetCyc¹ is

where the asterisk indicates the point of attachment to the E group and the wavy line indicates the point of attachment to the ring comprising X¹, X², X³ and X⁴;

E is

(a) hydrogen,

(d) C1-C6 alkyl optionally substituted with one to three fluoros,

(e) hydroxyC1-C6 alkyl- optionally substituted with one to three fluoros,

(h) (C1-C6 alkoxy)hydroxy C1-C6 alkyl-,

(i) (C1-C6 alkyl)C(═O)—, wherein said alkyl portion is optionally substituted with one to three fluoros, or said alkyl portion is substituted with R′R″N— or R′R″NCH₂— wherein R′ and R″ are independently H or C1-C6 alkyl,

(j) (hydroxy C1-C6 alkyl)C(═O)— optionally substituted with one to three fluoros,

(k) (C1-C6 alkoxy)C(═O)—,

(l) (C1-C6 alkoxy)(C1-C6 alkyl)C(═O)—,

(n) Cyc¹,

(o) Cyc¹C(═O)—,

(p) Cyc¹(C1-C6 alkyl)C(═O)— wherein the alkyl portion is optionally substituted with one or more groups independently selected from the group consisting of OH, fluoro, C1-C3 alkoxy and R^(c)R^(d)N—, where R^(c) and R^(d) are independently H or C1-C6 alkyl,

(q) hetCyc⁴,

(r) hetCyc⁴C(═O)—,

(s) hetCyc⁴(C1-C6 alkyl)C(═O)—,

(t) hetCyc⁴C(═O)C1-C6 alkyl-,

(w) Ar²C(═O)—,

(x) (Ar²)C1-C6 alkyl-,

(y) (Ar²)hydroxy C2-C6 alkyl-,

(z) Ar²(C1-C6 alkyl)C(═O)— wherein the alkyl portion is optionally substituted with one or two groups independently selected from the group consisting of OH, C1-C6 alkyl (optionally substituted with 1-3 fluoros), hydroxyC1-C6 alkyl, C1-C6 alkoxy, R^(e)R^(f)N— and (R^(e)R^(f)N)C1-C3 alkyl- wherein R^(e) and R^(f) are independently H or C1-C6 alkyl, or said alkyl portion is substituted with a 5-6 membered heterocyclic ring having one or two ring heteroatoms independently selected from N and O and wherein the heterocyclic ring is optionally substituted with C1-C6 alkyl,

(aa) hetAr²C(═O)—,

(bb) (hetAr²)hydroxy C2-C6 alkyl-,

(cc) hetAr²(C1-C6 alkyl)C(═O)— wherein the alkyl portion is optionally substituted with one or two groups independently selected from the group consisting of OH, C1-C6 alkyl, hydroxyC1-C6 alkyl, C1-C6 alkoxy, R^(e)R^(f)N— and (R^(e)R^(f)N)C1-C3 alkyl- wherein R^(e) and R^(f) are independently H or C1-C6 alkyl, or said alkyl portion is substituted with a 5-6 membered heterocyclic ring having one or two ring heteroatoms independently selected from N and O and wherein the heterocyclic ring is optionally substituted with C1-C6 alkyl,

(dd) R¹R²NC(═O)—,

(ee) R¹R²N(C1-C6 alkyl)C(═O)— wherein the alkyl portion is optionally substituted with phenyl,

(ff) R¹R²NC(═O)C1-C6 alkyl-,

(hh) CH₃SO₂(C1-C6 alkyl)C(═O)—,

(ii) (C1-C6 alkyl)SO₂—,

(jj) (C3-C6 cycloalkyl)CH₂SO₂—,

(kk) hetCyc⁵-SO₂—,

(ll) R⁴R⁵NSO₂—,

(oo) (hetAr²)C1-C6 alkyl-,

(pp) (hetCyc⁴)C1-C6 alkyl-,

(qq) (C1-C6 alkoxy)C1-C6 alkyl- wherein said alkoxy portion is optionally substituted with 1-3 fluoros,

(rr) (C3-C6 cycloalkoxy)C1-C6 alkyl-,

(ss) (C3-C6 cycloalkyl)C1-C6 alkyl-,

(tt) (R^(g)R^(h)N)C1-C6 alkyl- wherein R^(g) and R^(h) are independently H or C1-C6 alkyl,

(vv) (C1-C6 alkyl)SO₂C1-C6 alkyl-,

(ww) (C1-C6 alkoxy)C(═O)NHC1-C6 alkyl-,

(yy) (C3-C6 cycloalkyl)SO₂— wherein said cycloalkyl is optionally substituted with C1-C6 alkyl,

(aaa) (N—(C1-C3 alkyl)pyridinonyl)C1-C6 alkyl-, or

(bbb) (Ar⁴SO₂)C1-C6 alkyl-;

and hetCyc¹, Cyc¹, hetCyc⁴, Ar², hetAr², R¹, R², hetCyc⁵, R⁴, R⁵, and Ar⁴ are as defined for Formula I.

In one embodiment of Formula I-B, A is CN.

In one embodiment of Formula I-B, hetAr¹ is pyrazolyl optionally substituted with one or more substituents independently selected from the group consisting of C1-C6 alkyl (optionally substituted with one to three fluoros).

In one embodiment of Formula I-B, A is CN and hetAr¹ is pyrazolyl optionally substituted with one or more substituents independently selected from the group consisting of C1-C6 alkyl (optionally substituted with one to three fluoros).

In one embodiment of Formula I-B, E is (i) (C1-C6 alkyl)C(═O)—, wherein said alkyl portion is optionally substituted with one to three fluoros, or said alkyl portion is substituted with R′R″N— or R′R″NCH₂— wherein R′ and R″ are independently H or C1-C6 alkyl, (r) hetCyc⁴C(═O)— where hetCyc⁴ is as defined for Formula I, (z) Ar²(C1-C6 alkyl)C(═O)— wherein the alkyl portion is optionally substituted with one or two groups independently selected from the group consisting of OH, C1-C6 alkyl (optionally substituted with 1-3 fluoros), hydroxyC1-C6 alkyl, C1-C6 alkoxy, R^(e)R^(f)N— and (R^(e)R^(f)N)C1-C3 alkyl- wherein R^(e) and R^(f) are independently H or C1-C6 alkyl, or said alkyl portion is substituted with a 5-6 membered heterocyclic ring having one or two ring heteroatoms independently selected from N and O, wherein the heterocyclic ring is optionally substituted with C1-C6 alkyl, and where Ar² is as defined for Formula I, or (oo) (hetAr²)C1-C6 alkyl-, where hetAr² is as defined for Formula I.

In one embodiment of Formula I-B, E is (i) (C1-C6 alkyl)C(═O)—, wherein said alkyl portion is optionally substituted with one to three fluoros, or said alkyl portion is substituted with R′R″N— or R′R″NCH₂— wherein R′ and R″ are independently H or C1-C6 alkyl.

In one embodiment of Formula I-B, A is CN, hetAr¹ is pyrazolyl optionally substituted with one or more substituents independently selected from the group consisting of C1-C6 alkyl (optionally substituted with one to three fluoros), and E is (i) (C1-C6 alkyl)C(═O)—, wherein said alkyl portion is optionally substituted with one to three fluoros, or said alkyl portion is substituted with R′R″N— or R′R″NCH₂— wherein R′ and R″ are independently H or C1-C6 alkyl.

In one embodiment of Formula I-B, E is (r) hetCyc⁴C(═O)— where hetCyc⁴ is as defined for Formula I.

In one embodiment of Formula I-B, A is CN, hetAr¹ is pyrazolyl optionally substituted with one or more substituents independently selected from the group consisting of C1-C6 alkyl (optionally substituted with one to three fluoros), and E is (r) hetCyc⁴C(═O)— where hetCyc⁴ is as defined for Formula I.

In one embodiment of Formula I-B, E is (z) Ar²(C1-C6 alkyl)C(═O)— wherein the alkyl portion is optionally substituted with one or two groups independently selected from the group consisting of OH, C1-C6 alkyl (optionally substituted with 1-3 fluoros), hydroxyC1-C6 alkyl, C1-C6 alkoxy, R^(e)R^(f)N— and (R^(e)R^(f)N)C1-C3 alkyl- wherein R^(e) and R^(f) are independently H or C1-C6 alkyl, or said alkyl portion is substituted with a 5-6 membered heterocyclic ring having one or two ring heteroatoms independently selected from N and O, wherein the heterocyclic ring is optionally substituted with C1-C6 alkyl, and where Ar² is as defined for Formula I.

In one embodiment of Formula I-B, A is CN, hetAr¹ is pyrazolyl optionally substituted with one or more substituents independently selected from the group consisting of C1-C6 alkyl (optionally substituted with one to three fluoros), and E is (z) Ar²(C1-C6 alkyl)C(═O)— wherein the alkyl portion is optionally substituted with one or two groups independently selected from the group consisting of OH, C1-C6 alkyl (optionally substituted with 1-3 fluoros), hydroxyC1-C6 alkyl, C1-C6 alkoxy, R^(e)R^(f)N— and (R^(e)R^(f)N)C1-C3 alkyl- wherein R^(e) and R^(f) are independently H or C1-C6 alkyl, or said alkyl portion is substituted with a 5-6 membered heterocyclic ring having one or two ring heteroatoms independently selected from N and O, wherein the heterocyclic ring is optionally substituted with C1-C6 alkyl, and where Ar² is as defined for Formula I.

In one embodiment of Formula I-B, E is (oo) (hetAr²)C1-C6 alkyl-, where hetAr² is as defined for Formula I.

In one embodiment of Formula I-B, A is CN, hetAr¹ is pyrazolyl optionally substituted with one or more substituents independently selected from the group consisting of C1-C6 alkyl (optionally substituted with one to three fluoros), and E is (oo) (hetAr²)C1-C6 alkyl-, where hetCyc^(a) and hetAr² are as defined for Formula I.

In one embodiment, Formula I includes compounds of Formula I-C, wherein:

X¹ is N and each of X², X³ and X⁴ is CH;

A is CN;

B is hetAr¹;

hetAr¹ is pyrazolyl optionally substituted with one or more substituents independently selected from C1-C6 alkyl (optionally substituted with one to three fluoros), (C1-C6 alkoxy)C1-C6 alkyl-, (C1-C6 alkylSO₂)C1-C6 alkyl-, hetCyc^(a), and hetCyc^(a)C1-C6 alkyl;

R^(a) and R^(b) are independently H or C1-C6 alkyl;

hetCyc^(a) is a 4-6 membered heterocyclic ring having a ring heteroatom selected from N and O, wherein the heterocyclic ring is optionally substituted with halogen, C1-C6 alkyl (optionally substituted with one to three fluoros), (C1-C6 alkoxy)C1-C6 alkyl-, di(C1-C3 alkyl)NCH₂C(═O)—, (C1-C6 alkoxy)C(═O)— or (C1-C6 alkoxy)CH₂C(═O)—;

D is hetCyc¹;

hetCyc¹ is

where the asterisk indicates the point of attachment to the E group and the wavy line indicates the point of attachment to the ring comprising X¹, X², X³ and X⁴;

E is

(a) hydrogen,

(b) OH,

(c) R′R″N(CH₂)_(n)— wherein R′ is H or C1-C6 alkyl, R″ is H, C1-C6 alkyl or phenyl, and n is 0 or 1,

(f) C1-C6 alkoxy optionally substituted with one to three fluoros,

(g) hydroxyC1-C6 alkoxy- optionally substituted with one to three fluoros,

(k) (C1-C6 alkoxy)C(═O)—,

(m) HC(═O)—,

(r) hetCyc⁴C(═O)—,

(u) hetCyc⁴C(═O)NR^(g)—, where R^(g) is H or C1-C6 alkyl,

(v) Ar²,

(x) (Ar²)C1-C6 alkyl-,

(dd) R¹R²NC(═O)—,

(ff) R¹R²NC(═O)C1-C6 alkyl-,

(gg) R¹R²NC(═O)NH—,

(ll) R⁴R⁵NSO₂—,

(mm) R⁶C(═O)NH—,

(nn) hetCyc⁶,

(oo) (hetAr²)C1-C6 alkyl-,

(tt) (R^(g)R^(h)N)C1-C6 alkyl- wherein R^(g) and R^(h) are independently H or C1-C6 alkyl,

(uu) Ar²—O—, or

(ccc) hetAr²—O—,

where hetCyc⁴, Ar², R¹, R², R⁴, R⁵, R⁶, hetCyc⁶, and hetAr² are as defined for Formula I.

In one embodiment of Formula I-C, A is CN.

In one embodiment of Formula I-C, hetAr¹ is pyrazolyl optionally substituted with one or more substituents independently selected from the group consisting of C1-C6 alkyl (optionally substituted with one to three fluoros).

In one embodiment of Formula I-C, A is CN and hetAr¹ is pyrazolyl optionally substituted with one or more substituents independently selected from the group consisting of C1-C6 alkyl (optionally substituted with one to three fluoros).

In one embodiment of Formula I-C, E is (x) (Ar²)C1-C6 alkyl-, (mm) R⁶C(═O)NH—, or (ccc) hetAr²—O—.

In one embodiment of Formula I-C, A is CN, hetAr¹ is pyrazolyl optionally substituted with one or more substituents independently selected from the group consisting of C1-C6 alkyl (optionally substituted with one to three fluoros), and E is (x) (Ar²)C1-C6 alkyl-.

In one embodiment of Formula I-C, A is CN, hetAr¹ is pyrazolyl optionally substituted with one or more substituents independently selected from the group consisting of C1-C6 alkyl (optionally substituted with one to three fluoros), and E is (mm) R⁶C(═O)NH—.

In one embodiment of Formula I-C, A is CN, hetAr¹ is pyrazolyl optionally substituted with one or more substituents independently selected from the group consisting of C1-C6 alkyl (optionally substituted with one to three fluoros), and E is (ccc) hetAr²—O—.

In one embodiment, Formula I includes compounds of Formula I-D, wherein:

X¹ is N and each of X², X³ and X⁴ is CH;

A is CN;

B is hetAr¹;

hetAr¹ is pyrazolyl optionally substituted with one or more substituents independently selected from C1-C6 alkyl (optionally substituted with one to three fluoros), (C1-C6 alkoxy)C1-C6 alkyl-, (C1-C6 alkylSO₂)C1-C6 alkyl-, hetCyc^(a), and hetCyc^(a)C1-C6 alkyl;

R^(a) and R^(b) are independently H or C1-C6 alkyl;

hetCyc^(a) is a 4-6 membered heterocyclic ring having a ring heteroatom selected from N and O, wherein the heterocyclic ring is optionally substituted with halogen, C1-C6 alkyl (optionally substituted with one to three fluoros), (C1-C6 alkoxy)C1-C6 alkyl-, di(C1-C3 alkyl)NCH₂C(═O)—, (C1-C6 alkoxy)C(═O)— or (C1-C6 alkoxy)CH₂C(═O)—;

D is hetCyc²;

hetCyc² is:

where the asterisk indicates the point of attachment to the E group and the wavy line indicates the point of attachment to the ring comprising X¹, X², X³ and X⁴;

E is

(a) hydrogen,

(c) R′R″N(CH₂)_(n)— wherein R′ is H or C1-C6 alkyl, R″ is H, C1-C6 alkyl or phenyl, and n is 0 or 1;

(mm) R⁶C(═O)NH—, or

(oo) hetAr²C1-C6 alkyl-;

hetAr² is a 5-6 membered monocyclic heteroaryl ring having 1-3 ring heteroatoms independently selected from N, O and S or a 9-10 membered bicyclic heteroaryl ring having 1-2 ring nitrogen atoms, wherein hetAr² is optionally substituted with one or more substituents independently selected from the group consisting of halogen, C1-C6 alkyl (optionally substituted with one to three fluoros), C1-C6 alkoxy (optionally substituted with 1-3 fluoros), hydroxyC1-C6 alkyl, (C3-C6)cycloalkyl, (C1-C6 alkoxy)C1-C6 alkyl-, CN and R′R″N— where R′ and R″ are independently H or C1-C3 alkyl;

R⁶ is C1-C6 alkyl, hydroxyC1-C6 alkyl, C1-C6 alkoxy, (C1-C6 alkoxy)C1-C6 alkyl-, phenyl or hetCyc⁸; and

hetCyc⁸ is a 5-6 membered heterocyclic ring having a ring heteroatom selected from O and N, wherein the heterocyclic ring is optionally substituted with C1-C6 alkyl.

In one embodiment of Formula I-D, A is CN.

In one embodiment of Formula I-D, hetAr¹ is pyrazolyl optionally substituted with one or more substituents independently selected from the group consisting of C1-C6 alkyl (optionally substituted with one to three fluoros).

In one embodiment of Formula I-D, A is CN and hetAr¹ is pyrazolyl optionally substituted with one or more substituents independently selected from the group consisting of C1-C6 alkyl (optionally substituted with one to three fluoros).

In one embodiment of Formula I-D, hetCyc² is:

In one embodiment of Formula I-D, A is CN and hetCyc² is

In one embodiment of Formula I-D, A is CN, hetAr¹ is pyrazolyl optionally substituted with one or more substituents independently selected from the group consisting of C1-C6 alkyl (optionally substituted with one to three fluoros); and hetCyc² is

In one embodiment of Formula I-D, A is CN, hetAr¹ is pyrazolyl optionally substituted with one or more substituents independently selected from the group consisting of C1-C6 alkyl (optionally substituted with one to three fluoros); hetCyc² is

and E is (a) hydrogen.

In one embodiment of Formula I-D, A is CN, hetAr¹ is pyrazolyl optionally substituted with one or more substituents independently selected from the group consisting of C1-C6 alkyl (optionally substituted with one to three fluoros); hetCyc² is

and E is (c) R′R″N(CH₂)_(n)— wherein R′ is H or C1-C6 alkyl, R″ is H, C1-C6 alkyl or phenyl, and n is 0 or 1.

In one embodiment of Formula I-D, A is CN, hetAr¹ is pyrazolyl optionally substituted with one or more substituents independently selected from the group consisting of C1-C6 alkyl (optionally substituted with one to three fluoros); hetCyc² is

and E is (mm) R⁶C(═O)NH—.

In one embodiment of Formula I-D, A is CN, hetAr¹ is pyrazolyl optionally substituted with one or more substituents independently selected from the group consisting of C1-C6 alkyl (optionally substituted with one to three fluoros); and hetCyc² is

and E is (oo) hetAr²C1-C6 alkyl-.

It will be appreciated that certain compounds provided herein may contain one or more centers of asymmetry and may therefore be prepared and isolated in a mixture of isomers such as a racemic mixture, or in an enantiomerically pure form.

It will further be appreciated that the compounds of Formula I or their salts may be isolated in the form of solvates, and accordingly that any such solvate is included within the scope of the present invention. For example, compounds of Formula I and salts thereof can exist in unsolvated as well as solvated forms with pharmaceutically acceptable solvents such as water, ethanol, and the like.

The compounds of Formula I include pharmaceutically acceptable salts thereof. In addition, the compounds of Formula I also include other salts of such compounds which are not necessarily pharmaceutically acceptable salts, and which may be useful as intermediates for preparing and/or purifying compounds of Formula I and/or for separating enantiomers of compounds of Formula I. Non-limiting examples of salts include monochloride, dichloride, trifluoroacetic acid, and di-trifluoroacetic acid salts of compounds of Formula I.

In one embodiment, the compounds of Formula I include the compounds of Examples 1-121 and stereoisomers and pharmaceutically acceptable salts and solvates thereof. In one embodiment, the compounds of Examples 1-121 are in the free base form. In one embodiment, the compounds of Examples 1-121 are monochloride, dichloride, trifluoroacetic acid, or di-trifluoroacetic acid salts.

The term “pharmaceutically acceptable” indicates that the substance or composition is compatible chemically and/or toxicologically, with the other ingredients comprising a formulation, and/or the patient being treated therewith.

Compounds provided herein may also contain unnatural proportions of atomic isotopes at one or more of the atoms that constitute such compounds. That is, an atom, in particular when mentioned in relation to a compound according to Formula I, comprises all isotopes and isotopic mixtures of that atom, either naturally occurring or synthetically produced, either with natural abundance or in an isotopically enriched form. For example, when hydrogen is mentioned, it is understood to refer to ¹H, ²H, ³H or mixtures thereof; when carbon is mentioned, it is understood to refer to ¹¹C, ¹²C, ¹³C, ¹⁴C or mixtures thereof; when nitrogen is mentioned, it is understood to refer to ¹³N, ¹⁴N, ¹⁵N or mixtures thereof; when oxygen is mentioned, it is understood to refer to ¹⁴O, ¹⁵O, ¹⁶O, ¹⁷O, ¹⁸O or mixtures thereof; and when fluoro is mentioned, it is understood to refer to ¹⁸F, ¹⁹F or mixtures thereof. The compounds provided herein therefore also comprise compounds with one or more isotopes of one or more atom, and mixtures thereof, including radioactive compounds, wherein one or more non-radioactive atoms has been replaced by one of its radioactive enriched isotopes. Radiolabeled compounds are useful as therapeutic agents, e.g., cancer therapeutic agents, research reagents, e.g., assay reagents, and diagnostic agents, e.g., in vivo imaging agents. All isotopic variations of the compounds provided herein, whether radioactive or not, are intended to be encompassed within the scope of the present invention.

For illustrative purposes, Schemes 1-4 show general methods for preparing the compounds provided herein as well as key intermediates. For a more detailed description of the individual reaction steps, see the Examples section below. Those skilled in the art will appreciate that other synthetic routes may be used to synthesize the inventive compounds. Although specific starting materials and reagents are depicted in the Schemes and discussed below, other starting materials and reagents can be easily substituted to provide a variety of derivatives and/or reaction conditions. In addition, many of the compounds prepared by the methods described below can be further modified in light of this disclosure using conventional chemistry well known to those skilled in the art.

Scheme 1 shows a general scheme for the synthesis of compound 13 where A is CN, and B, X¹, X², X³, X⁴, and E are as defined for Formula I, and the D ring is as defined for hetCyc¹, hetCyc², hetCyc³ or hetCyc⁹ of Formula I, and the synthesis of compound 13a where A is CN, D is as defined for Formula I provided that the D ring is coupled to the ring defined by X¹, X², X³ and X⁴ through a ring nitrogen atom in the D ring, X¹, X², X³, X⁴ provided that at least one of X¹ and X² is nitrogen, and B, X³, X⁴, and E are as defined for Formula I.

Compound 2 is obtained by treating MSH reagent with 3-bromo-5-methoxypyridine, which is commercially available. The aminating reagent O-mesitylsulfonylhydroxylamine (MSH) may be prepared as described in Mendiola, J., et al., Org. Process Res. Dev. 2009, 13(2), 263-267. Compound 2 may be reacted with ethyl propiolate to provide the pyrazolo[1,5-a]pyrazine a mixture of compounds 3A and 3B, which typically are obtained in a ratio of approximately 2:1 to 9:1. The mixture of compounds 3A and 3B may be treated with 48% HBr at elevated temperatures, followed by recrystallization or chromatography purifications to isolate compound 4A as the minor isomer and compound 4B as the major isomer.

The isolated compound 4B may be functionalized with a formyl group using POCl₃ followed by purification to provide compound 5. The formyl group of compound 5 may be converted to an oxime group using NH₂OH to provide compound 6. The oxime group of compound 6 may be converted to a nitrile group using acetic anhydride to provide compound 7. The B group may be installed by treating compound 7 with a corresponding boronic ester having the formula hetAr¹—B(OR^(a))(OR^(b)) where hetAr¹ is as defined for Formula I and R^(a) and R^(b) are H or (1-6C)alkyl, or R^(a) and R^(b) together with the atoms to which they are connected form a 5-6 membered ring optionally substituted with 1-4 substituents selected from (C1-C3 alkyl), using appropriate palladium-catalyzed cross-coupling reaction conditions, e.g., Suzuki coupling reaction conditions (for example, a palladium catalyst and optionally a ligand in the presence of an inorganic base, for example, Pd₂(dba)₃, X-Phos and Na₂CO₃ in dioxane at elevated temperatures) to provide compound 8 where B is hetAr¹ as defined for Formula I. The methoxy group of compound 8 may be converted to a hydroxy group by treating compound 8 with aluminum trichloride to provide compound 9. The free hydroxy group of compound 9 may be converted to a triflate group by treating compound 9 with a triflating reagent, for example 1,1,1-trifluoro-N-phenyl-N-((trifluoromethyl)sulfonyl)methanesulfonamide to provide compound 10. Compound 12 may be prepared by coupling compound 10 with the corresponding boronic ester compound 11 where Z is —B(OR^(a))(OR^(b)) and R^(a) and R^(b) are H or (1-6C)alkyl, or R^(a) and R^(b) together with the atoms to which they are connected form a 5-6 membered ring optionally substituted with 1-4 substituents selected from (C1-C3 alkyl), using appropriate palladium-catalyzed cross-coupling reaction conditions, e.g., Suzuki coupling reaction conditions (for example, a palladium catalyst and optionally a ligand in the presence of an inorganic base, for example, Pd₂(dba)₃, X-Phos and Na₂CO₃ in dioxane at elevated temperatures), wherein if the D ring of compound 11 comprises an unsubstituted ring nitrogen atom, the nitrogen atom is protected with an appropriate amine protecting group prior to coupling. The protecting group if present on the D ring of compound 12 may be removed under standard conditions (for example, a Boc protecting group may be removed by treating compound 12 under acidic conditions, e.g., using HCl) to provide compound 13 where E is H. Alternatively, the deprotected D ring may be functionalized to install the E group under standard conditions such as described below to provide compound 13 where E is as defined for Formula I except that E is not H.

Alternatively, compound 10 may be coupled with compound 14 using appropriate palladium-catalyzed cross-coupling reaction conditions, e.g., Suzuki coupling reaction conditions (for example, a palladium catalyst and optionally a ligand in the presence of an inorganic base, for example, Pd(PPh₃)₄ and Na₂CO₃) to provide compound 15. Compound 15 may be reacted with compound 16 under appropriate S_(N)Ar conditions (for example, optionally in the presence of a base such as K₂CO₃ and at elevated temperature) to provide compound 12a, wherein if the D ring of compound 16 comprises a second unsubstituted ring nitrogen atom, the second nitrogen atom is protected with an appropriate amine protecting group prior to coupling. The protecting group if present on the D ring of compound 12a may be removed under standard conditions (for example, a Boc group may be removed by treating compound 12a to acidic conditions, e.g., HCl) to provide compound 13a where E is H. Alternatively, the deprotected D ring may be functionalized to install the E group under standard conditions such as described below to provide compound 13a where E is as defined for Formula I except that E is not H.

Scheme 2 shows an alternative route for the synthesis of compound 13, wherein A is CN, and B, X¹, X², X³, X⁴, and E are as defined for Formula I, and the D ring is as defined for hetCyc¹, hetCyc², hetCyc³ or hetCyc⁹ of Formula I. Compound 4A (prepared as in Scheme 1) may be functionalized with a formyl group using POCl₃ to provide compound 17. The formyl group may be converted to an oxime group using NH₂OH to provide compound 18. The oxime group may be converted to a nitrile group using acetic anhydride to provide compound 19. The methoxy group of compound 19 may be converted to a hydroxy group by treating compound 19 with aluminum trichloride to provide compound 20. Compound 21 may be prepared by coupling compound 20 with the corresponding boronic ester compound 11 where Z is —B(OR^(a))(OR^(b)) and R^(a) and R^(b) are H or (1-6C)alkyl, or R^(a) and R^(b) together with the atoms to which they are connected form a 5-6 membered ring optionally substituted with 1-4 substituents selected from (C1-C3 alkyl), using appropriate palladium-catalyzed cross-coupling reaction conditions, e.g., Suzuki coupling reaction conditions (for example, a palladium catalyst and optionally a ligand in the presence of an inorganic base, for example, Pd(PPh₃)₄ and Na₂CO₃ in dioxane at elevated temperatures), wherein if the D ring of compound 11 comprises an unsubstituted ring nitrogen atom, the nitrogen atom is protected with an appropriate amine protecting group prior to coupling. The free hydroxy group of compound 21 may be converted to a triflate group by treating compound 21 with a triflating reagent, for example 1,1,1-trifluoro-N-phenyl-N-((trifluoromethyl)sulfonyl)methanesulfonamide to provide compound 22. The B group may be installed by treating compound 22 with the corresponding boronic ester having the formula hetAr¹—B(OR^(a))(OR^(b)) where hetAr¹ is as defined for Formula I and R^(a) and R^(b) are H or (1-6C)alkyl, or R^(a) and R^(b) together with the atoms to which they are connected form a 5-6 membered ring optionally substituted with 1-4 substituents selected from (C1-C3 alkyl), using appropriate palladium-catalyzed cross-coupling reaction conditions, e.g., Suzuki coupling reaction conditions (for example, a palladium catalyst and optionally a ligand in the presence of an inorganic base, for example, Pd₂(dba)₃, X-Phos and Na₂CO₃ in dioxane at elevated temperatures) to provide compound 12 where B is hetAr¹ as defined for Formula I. The protecting group if present on the D ring of compound 12 may be removed under standard conditions (for example, a Boc group may be removed by treating compound 12 to acidic conditions, e.g., HCl in propan-2-ol) to provide compound 13 where E is H. Alternatively, the deprotected D ring may be functionalized to install the E group under standard conditions such as described below to provide compound 13 where E is as defined for Formula I except that E is not H.

Scheme 3 shows a general scheme for the synthesis of compound 28 where A is Cl, and B, X¹, X², X³, X⁴, and E are as defined for Formula I, and the D ring is as defined for hetCyc¹, hetCyc², hetCyc³ or hetCyc⁹ of Formula I. Compound 4B (prepared as in Scheme 1) may be chlorinated using N-chlorosuccinimide to provide compound 23. The B group may be installed by coupling compound 23 with an appropriate boronic ester having the formula hetAr¹—B(OR^(a))(OR^(b)) where hetAr¹ is as defined for Formula I and R^(a) and R^(b) are H or (1-6C)alkyl, or R^(a) and R^(b) together with the atoms to which they are connected form a 5-6 membered ring optionally substituted with 1-4 substituents selected from (C1-C3 alkyl), under appropriate palladium-catalyzed cross-coupling reaction conditions, e.g., Suzuki coupling reaction conditions (for example, a palladium catalyst and optionally a ligand in the presence of an inorganic base, for example, Pd(PPh₃)₄ and Na₂CO₃ in dioxane at elevated temperatures) to provide compound 24 where B is hetAr¹ as defined for Formula I. The methoxy group of compound 24 may be converted to a hydroxy group under standard conditions, for example by treating compound 24 with BBr₃, to yield compound 25. The free hydroxy group of compound 25 may be converted to a triflate group by treating compound 25 with an appropriate triflating reagent in the presence of a base, e.g., 1,1,1-trifluoro-N-phenyl-N-((trifluoromethyl)sulfonyl)methanesulfonamide and DIEA to provide compound 26. Compound 27 may be prepared by coupling compound 26 with the corresponding boronic ester compound 11 where Z is —B(OR^(a))(OR^(b)) and R^(a) and R^(b) are H or (1-6C)alkyl, or R^(a) and R^(b) together with the atoms to which they are connected form a 5-6 membered ring optionally substituted with 1-4 substituents selected from (C1-C3 alkyl), using under standard coupling conditions, e.g., Suzuki coupling reaction conditions (for example, a palladium catalyst and optionally a ligand in the presence of an inorganic base, for example, Pd(PPh₃)₄ and Na₂CO₃ in dioxane at elevated temperatures), wherein if the D ring of compound 11 comprises an unsubstituted ring nitrogen atom, the nitrogen atom is protected with an appropriate amine protecting group prior to coupling. The protecting group if present on the D ring of compound 27 may be removed under standard conditions (for example, a Boc group may be removed by treating compound 27 with acid (e.g., 5-6 N HCl in propan-2-ol) to provide compound 28 where E is H. Alternatively, the deprotected D ring may be functionalized to install the E group under standard conditions such as described below to provide compound 28 where E is as defined for Formula I except that E is not H.

Scheme 4 shows a general scheme for the synthesis of compound 33, wherein A is H, and B, X¹, X², X³, X⁴, D and E are as defined for Formula I. Compound 4B (prepared as in Scheme 1) may be coupled with an appropriate boronic ester having the formula hetAr¹—B(OR^(a))(OR^(b)) where hetAr¹ is as defined for Formula I and R^(a) and R^(b) are H or (1-6C)alkyl, or R^(a) and R^(b) together with the atoms to which they are connected form a 5-6 membered ring optionally substituted with 1-4 substituents selected from (C1-C3 alkyl), under appropriate palladium-catalyzed cross-coupling reaction conditions, e.g., Suzuki coupling reaction conditions (for example, a palladium catalyst and optionally a ligand in the presence of an inorganic base, for example, Pd(PPh₃)₄ and Na₂CO₃ in dioxane at elevated temperatures) to install the B group to provide compound 29 where B is hetAr¹ as defined for Formula I. The methoxy group of compound 29 may be converted to a hydroxy group by treating compound 29 with aluminum trichloride to provide compound 30. The free hydroxy group of compound 30 may be converted to a triflate group by treating compound 33 with a triflating reagent in the presence of a base, e.g., 1,1,1-trifluoro-N-phenyl-N-((trifluoromethyl)sulfonyl)methanesulfonamide and DIEA in an appropriate solvent such as THF to provide compound 31. Compound 32 may be prepared by coupling compound 31 with compound 11 under appropriate palladium-catalyzed cross-coupling reaction conditions, e.g., Suzuki coupling reaction conditions (for example, a palladium catalyst and optionally a ligand in the presence of an inorganic base, for example, Pd(PPh₃)₄ and Na₂CO₃ in dioxane at elevated temperatures), wherein if the D ring of compound 11 comprises an unsubstituted ring nitrogen atom, the nitrogen atom is protected with an appropriate amine protecting group prior to coupling. The protecting group if present on the D ring of compound 32 may be removed under standard conditions (for example, a Boc group may be removed by treating compound 32 under acidic conditions, e.g., HCl in propan-2-ol) to provide compound 33 where E is H. Alternatively, the deprotected D ring may be functionalized to install the E group under standard conditions such as described below to provide compound 33 where E is as defined for Formula I except that E is not H.

The D ring of any one of compounds 13, 13a, 28, and 33 described in Schemes 1-4 may be functionalized to install an E group, where E is any of the E groups defined for Formula I with the exception of hydrogen, using standard chemistry well known to persons skilled in the art.

For example, an amide derivative (e.g., where D is hetCyc¹ where hetCyc¹ is piperazinyl and E is (C1-C6 alkyl)C(═O)— optionally substituted with one to three fluoros; (hydroxy C1-C6 alkyl)C(═O)— optionally substituted with one to three fluoros; (C1-C6 alkoxy)(C1-C6 alkyl)C(═O)—; Cyc¹C(═O)—; Cyc¹(C1-C6 alkyl)C(═O)—; hetCyc⁴(C1-C6 alkyl)C(═O)—; Ar²C(═O)—; Ar²(C1-C6 alkyl)C(═O)— wherein the alkyl portion is optionally substituted with one or two groups independently selected from the group consisting of OH, C1-C6 alkyl, hydroxyC1-C6 alkyl-, (C1-C6)alkoxy, R^(e)R^(f)N— and (R^(e)R^(f)N)C1-C3 alkyl-, where R^(e) and R^(f) are independently selected from H and C1-C6 alkyl, or said alkyl portion is substituted with a 5-6 membered heterocyclic ring having one or two ring heteroatoms independently selected from N and O and wherein the heterocyclic ring is optionally substituted with C1-C6 alkyl; hetAr²C(═O)—; or hetAr²(C1-C6 alkyl)C(═O)— wherein the alkyl portion is optionally substituted with one or two groups independently selected from the group consisting of OH, C1-C6 alkyl, hydroxyC1-C6 alkyl-, (C1-C6)alkoxy, R^(e)R^(f)N— and (R^(e)R^(f)N)C1-C3 alkyl-, where R^(e) and R^(f) are independently H or C1-C6 alkyl), or said alkyl portion is substituted with a 5-6 membered heterocyclic ring having one or two ring heteroatoms independently selected from N and O and wherein the heterocyclic ring is optionally substituted with C1-C6 alkyl, may be obtained by treating compound 13 having a deprotected amino D ring with an carboxylic acid using conventional amide bond formation conditions, for example by treating the carboxylic acid with an activating agent (e.g., HATU), followed by addition of the compound 13 having a deprotected amino D ring in the presence of a base (e.g., an amine base such as DIEA) in an appropriate solvent (such as DMA) to provide a functionalized compound 13. The same chemistry may be utilized with compounds 13a, 28 and 33 to prepare functionalized compounds 13a, 28 and 33, respectively.

As another example, a urea derivative (e.g., where D is hetCyc¹ where hetCyc¹ is piperazinyl and E is hetCyc⁴C(═O)— or R¹R²NC(═O)—) may be prepared by first activating a ring nitrogen in the D ring of compound 13 with triphosgene in the presence of DIEA and in a solvent such as DCM, followed by addition of a primary or secondary amine reagent to provide a functionalized compound 13. The same chemistry may be utilized with compounds 13a, 28 and 33 to prepare functionalized compounds 13a, 28 and 33, respectively.

As another example, an N-alkyl derivative (e.g., where D is hetCyc¹ where hetCyc¹ is piperazinyl and E is hydroxyC1-C6 alkyl- optionally substituted with one to three fluoros; (C1-C6 alkoxy)(hydroxy C1-C6 alkyl); (Ar²)C1-C6 alkyl-; (Ar²)hydroxy C2-C6 alkyl-; or (hetAr²)hydroxyC2-C6 alkyl-; may be prepared by treating compound 13 where E is H with an alkyl bromide, alkyl chloride or epoxide in the presence of a base such as DIEA in a solvent at ambient or elevated temperatures) to provide a functionalized compound 13. The same chemistry may be utilized with compounds 13a, 28 and 33 to prepare functionalized compounds 13a, 28 and 33, respectively.

As another example, a sulfonamide derivative may be prepared by treating compound 13 where E is H with an appropriate sulfonyl chloride in the presence of a base, such as an amine base (such as triethylamine) in an appropriate solvent to provide a functionalized compound 13. The same chemistry may be utilized with compounds 13a, 28 and 33 to prepare functionalized compounds 13a, 28 and 33, respectively.

Further provided herein is a process for preparing of a compound of Formula I or a pharmaceutically acceptable salt thereof as defined herein which comprises:

(a) for a compound of Formula I where E is H and A, B, X¹, X², X³, X⁴, and D are as defined for Formula I, coupling a corresponding compound having the formula

where A and B are as defined for Formula I, with a corresponding compound having the formula 11

in the presence of a palladium catalyst and optionally a ligand and in the presence of a base, where Z is —B(OR^(a))(OR^(b)) and R^(a) and R^(b) are H or (1-6C)alkyl, or R^(a) and R^(b) together with the atoms to which they are connected form a 5-6 membered ring optionally substituted with 1-4 substituents selected from (C1-C3 alkyl), the

ring is as defined for hetCyc¹, hetCyc², hetCyc³ or hetCyc⁹ of Formula I, and X¹, X², X³ and X⁴ are as defined for Formula I, followed by removal of a protecting group on the D ring if present; or

(b) for a compound of Formula I where A, B, X¹, X², X³, X⁴, D and E are as defined for Formula I with the exception that E is not hydrogen, functionalizing a corresponding compound having the formula

wherein the

moiety is as defined for hetCyc¹, hetCyc², hetCyc³ or hetCyc⁹ of Formula I, and A, B, X¹, X², X³ and X⁴ are as defined for Formula I; or

(c) for a compound of Formula I where A is CN, D is as defined for Formula I provided that the D ring is coupled to the ring defined by X¹, X², X³ and X⁴ through a ring nitrogen atom in the D ring, X¹, X², X³, X⁴ provided that at least one of X¹ and X² is nitrogen, and E are as defined for Formula I, reacting a corresponding compound having the formula 15

where B, X¹, X², X³ and X⁴ are as defined for Formula I provided that at least one of X¹ and X² is nitrogen, with a corresponding compound having the formula 17

in the presence of a base, wherein the

ring is as defined for hetCyc¹, hetCyc², hetCyc³ or hetCyc⁹ of Formula I; or

(d) for a compound of Formula I where A is CN, E is H, and B, X¹, X², X³, X⁴, and D are as defined for Formula I, reacting a compound having the formula 22

wherein the

moiety is as defined for hetCyc¹, hetCyc², hetCyc³ or hetCyc⁹ in claim 1 and A, B, X¹, X², X³ and X⁴ are as defined for Formula I, with a corresponding compound having the formula

where hetAr¹ is as defined for Formula I and R^(a) and R^(b) are H or (1-6C)alkyl, or R^(a) and R^(b) together with the atoms to which they are connected form a 5-6 membered ring optionally substituted with 1-4 substituents selected from (C1-C3 alkyl), in the presence of a palladium catalyst and optionally a ligand and in the presence of a base; and

removing any protecting groups and optionally forming a pharmaceutically acceptable salt thereof.

Referring to processes (a) and (d), suitable palladium catalysts include Pd(PPh₃)₄, Pd₂(dba)₃, Pd(OAc)₂, and Pd(PPh₃)₂Cl₂. Suitable ligands include X-PHOS (2-dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl), DIPHOS (1,2-Bis(diphenylphosphino)ethane) or rac-BINAP (racemic-2,2′-Bis(diphenylphosphino)-1,1′-binaphthyl). The base may be, for example, an alkali metal carbonate, hydroxide, alkoxide or acetate, such as for example cesium carbonate, sodium carbonate, potassium carbonate, sodium hydroxide, sodium tert-butoxide or potassium acetate. Convenient solvents include aprotic solvents such as ethers (for example tetrahydrofuran or p-dioxane), toluene, DMF or DME. The reaction can be conveniently performed at a temperature ranging from ambient temperature to 120° C., for example from 80 to 110° C.

The ability of test compounds to act as RET inhibitors may be demonstrated by the assay described in Example A. IC₅₀ values are shown in Table 5.

In some embodiments, the compounds provided herein exhibit potent and selective RET inhibition. For example, the compounds provided herein exhibit nanomolar potency against wild type RET and select RET mutants, including, for example, the KIF5B-RET fusion, G810R and G810S ATP cleft front or linker mudations, M918T kinase domain, and V804M, V804L, and V804E gatekeeper mutations, with minimal activity against related kinases.

In some embodiments, the compounds of Formula I or a pharmaceutically acceptable salt or solvate thereof, selectively target a RET kinase. For example, a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof, can selectively target a RET kinase over another kinase or non-kinase target.

In some embodiments, a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof, exhibits at least a 30-fold selectivity for a RET kinase over another kinase. For example, a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof, exhibits at least a 40-fold selectivity; at least a 50-fold selectivity; at least a 60-fold selectivity; at least a 70-fold selectivity; at least a 80-fold selectivity; at least a 90-fold selectivity; at least 100-fold selectivity; at least 200-fold selectivity; at least 300-fold selectivity; at least 400-fold selectivity; at least 500-fold selectivity; at least 600-fold selectivity; at least 700-fold selectivity; at least 800-fold selectivity; at least 900-fold selectivity; or at least 1000-fold selectivity for a RET kinase over another kinase. In some embodiments, selectivity for a RET kinase over another kinase is measured in a cellular assay (e.g., a cellular assay as provided herein).

In some embodiments, the compounds provided herein can exhibit selectivity for a RET kinase over a KDR kinase (e.g., VEGFR2). In some embodiments, the selectivity for a RET kinase over a KDR kinase is observed without loss of potency for a RET kinase encoded by a RET gene including an activating mutation or a RET kinase inhibitor resistance mutation (e.g., a gatekeeper mutant). In some embodiments, the selectivity over a KDR kinase is at least 10-fold (e.g., at least a 40-fold selectivity; at least a 50-fold selectivity; at least a 60-fold selectivity; at least a 70-fold selectivity; at least a 80-fold selectivity; at least a 90-fold selectivity; at least 100-fold selectivity; at least 150-fold selectivity; at least 200-fold selectivity; at least 250-fold selectivity; at least 300-fold selectivity; at least 350-fold selectivity; or at least 400-fold selectivity) as compared to the inhibition of KIF5B-RET (i.e. the compounds were more potent against KIF5B-RET than KDR). In some embodiments, the selectivity for a RET kinase over a KDR kinase is about 30-fold. In some embodiments, the selectivity for a RET kinase over a KDR kinase is at least 100-fold. In some embodiments, the selectivity for a RET kinase over a KDR kinase is at least 150-fold. In some embodiments, the selectivity for a RET kinase over a KDR kinase is at least 400-fold. Without being bound by any theory, potent KDR kinase inhibition is believed to be a common feature among multikinase inhibitors (MKIs) that target RET and may be the source of the dose-limiting toxicities observed with such compounds.

In some embodiments, inhibition of V804M was similar to that observed for wild-type RET. For example, inhibition of V804M was within about 2-fold (e.g., about 5-fold, about 7-fold, about 10-fold) of inhibition of wild-type RET (i.e. the compounds were similarly potent against wild-type RET and V804M). In some embodiments, selectivity for a wildtype or V804M RET kinase over another kinase is measured in an enzyme assay (e.g., an enzyme assay as provided herein). In some embodiments, the compounds provided herein exhibit selective cytotoxicity to RET-mutant cells.

In some embodiments, the compounds provided herein exhibit brain and/or central nervous system (CNS) penetrance. Such compounds are capable of crossing the blood brain barrier and inhibiting a RET kinase in the brain and/or other CNS structures. In some embodiments, the compounds provided herein are capable of crossing the blood brain barrier in a therapeutically effective amount. For example, treatment of a patient with cancer (e.g., a RET-associated cancer such as a RET-associated brain or CNS cancer) can include administration (e.g., oral administration) of the compound to the patient. In some such embodiments, the compounds provided herein are useful for treating a primary brain tumor or metastatic brain tumor.

In some embodiments, the compounds of Formula I or a pharmaceutically acceptable salt or solvate thereof, exhibit one or more of high GI absorption, low clearance, and low potential for drug-drug interactions.

Compounds of Formula I are useful for treating diseases and disorders which can be treated with a RET kinase inhibitor, such as RET-associated diseases and disorders, e.g., proliferative disorders such as cancers, including hematological cancers and solid tumors, and gastrointestinal disorders such as IBS.

As used herein, terms “treat” or “treatment” refer to therapeutic or palliative measures. Beneficial or desired clinical results include, but are not limited to, alleviation, in whole or in part, of symptoms associated with a disease or disorder or condition, diminishment of the extent of disease, stabilized (i.e., not worsening) state of disease, delay or slowing of disease progression, amelioration or palliation of the disease state (e.g., one or more symptoms of the disease), and remission (whether partial or total), whether detectable or undetectable. “Treatment” can also mean prolonging survival as compared to expected survival if not receiving treatment.

As used herein, the terms “subject,” “individual,” or “patient,” are used interchangeably, refers to any animal, including mammals such as mice, rats, other rodents, rabbits, dogs, cats, swine, cattle, sheep, horses, primates, and humans. In some embodiments, the patient is a human. In some embodiments, the subject has experienced and/or exhibited at least one symptom of the disease or disorder to be treated and/or prevented. In some embodiments, the subject has been identified or diagnosed as having a cancer with a dysregulation of a RET gene, a RET protein, or expression or activity, or level of any of the same (a RET-associated cancer) (e.g., as determined using a regulatory agency-approved, e.g., FDA-approved, assay or kit). In some embodiments, the subject has a tumor that is positive for a dysregulation of a RET gene, a RET protein, or expression or activity, or level of any of the same (e.g., as determined using a regulatory agency-approved assay or kit). The subject can be a subject with a tumor(s) that is positive for a dysregulation of a RET gene, a RET protein, or expression or activity, or level of any of the same (e.g., identified as positive using a regulatory agency-approved, e.g., FDA-approved, assay or kit). The subject can be a subject whose tumors have a dysregulation of a RET gene, a RET protein, or expression or activity, or a level of the same (e.g., where the tumor is identified as such using a regulatory agency-approved, e.g., FDA-approved, kit or assay). In some embodiments, the subject is suspected of having a RET-associated cancer. In some embodiments, the subject has a clinical record indicating that the subject has a tumor that has a dysregulation of a RET gene, a RET protein, or expression or activity, or level of any of the same (and optionally the clinical record indicates that the subject should be treated with any of the compositions provided herein). In some embodiments, the patient is a pediatric patient.

The term “pediatric patient” as used herein refers to a patient under the age of 21 years at the time of diagnosis or treatment. The term “pediatric” can be further be divided into various subpopulations including: neonates (from birth through the first month of life); infants (1 month up to two years of age); children (two years of age up to 12 years of age); and adolescents (12 years of age through 21 years of age (up to, but not including, the twenty-second birthday)). Berhman R E, Kliegman R, Arvin A M, Nelson W E. Nelson Textbook of Pediatrics, 15th Ed. Philadelphia: W.B. Saunders Company, 1996; Rudolph A M, et al. Rudolph's Pediatrics, 21st Ed. New York: McGraw-Hill, 2002; and Avery M D, First L R. Pediatric Medicine, 2nd Ed. Baltimore: Williams & Wilkins; 1994. In some embodiments, a pediatric patient is from birth through the first 28 days of life, from 29 days of age to less than two years of age, from two years of age to less than 12 years of age, or 12 years of age through 21 years of age (up to, but not including, the twenty-second birthday). In some embodiments, a pediatric patient is from birth through the first 28 days of life, from 29 days of age to less than 1 year of age, from one month of age to less than four months of age, from three months of age to less than seven months of age, from six months of age to less than 1 year of age, from 1 year of age to less than 2 years of age, from 2 years of age to less than 3 years of age, from 2 years of age to less than seven years of age, from 3 years of age to less than 5 years of age, from 5 years of age to less than 10 years of age, from 6 years of age to less than 13 years of age, from 10 years of age to less than 15 years of age, or from 15 years of age to less than 22 years of age.

In certain embodiments, compounds of Formula I are useful for preventing diseases and disorders as defined herein (for example, autoimmune diseases, inflammatory diseases, and cancer). The term “preventing” as used herein means the prevention of the onset, recurrence or spread, in whole or in part, of the disease or condition as described herein, or a symptom thereof.

The term “RET-associated disease or disorder” as used herein refers to diseases or disorders associated with or having a dysregulation of a RET gene, a RET kinase (also called herein RET kinase protein), or the expression or activity or level of any (e.g., one or more) of the same (e.g., any of the types of dysregulation of a RET gene, a RET kinase, a RET kinase domain, or the expression or activity or level of any of the same described herein). Non-limiting examples of a RET-associated disease or disorder include, for example, cancer and gastrointestinal disorders such as irritable bowel syndrome (IBS).

The term “RET-associated cancer” as used herein refers to cancers associated with or having a dysregulation of a RET gene, a RET kinase (also called herein RET kinase protein), or expression or activity, or level of any of the same. Non-limiting examples of a RET-associated cancer are described herein.

The phrase “dysregulation of a RET gene, a RET kinase, or the expression or activity or level of any of the same” refers to a genetic mutation (e.g., a chromosomal translocation that results in the expression of a fusion protein including a RET kinase domain and a fusion partner, a mutation in a RET gene that results in the expression of a RET protein that includes a deletion of at least one amino acid as compared to a wildtype RET protein, a mutation in a RET gene that results in the expression of a RET protein with one or more point mutations as compared to a wildtype RET protein, a mutation in a RET gene that results in the expression of a RET protein with at least one inserted amino acid as compared to a wildtype RET protein, a gene duplication that results in an increased level of RET protein in a cell, or a mutation in a regulatory sequence (e.g., a promoter and/or enhancer) that results in an increased level of RET protein in a cell), an alternative spliced version of a RET mRNA that results in a RET protein having a deletion of at least one amino acid in the RET protein as compared to the wild-type RET protein), or increased expression (e.g., increased levels) of a wildtype RET kinase in a mammalian cell due to aberrant cell signaling and/or dysregulated autocrine/paracrine signaling (e.g., as compared to a control non-cancerous cell). As another example, a dysregulation of a RET gene, a RET protein, or expression or activity, or level of any of the same, can be a mutation in a RET gene that encodes a RET protein that is constitutively active or has increased activity as compared to a protein encoded by a RET gene that does not include the mutation. For example, a dysregulation of a RET gene, a RET protein, or expression or activity, or level of any of the same, can be the result of a gene or chromosome translocation which results in the expression of a fusion protein that contains a first portion of RET that includes a functional kinase domain, and a second portion of a partner protein (i.e., that is not RET). In some examples, dysregulation of a RET gene, a RET protein, or expression or activity or level of any of the same can be a result of a gene translocation of one RET gene with another non-RET gene. Non-limiting examples of fusion proteins are described in Table 1. Non-limiting examples of RET kinase protein point mutations/insertions/deletions are described in Tables 2 and 2a. Additional examples of RET kinase protein mutations (e.g., point mutations) are RET inhibitor resistance mutations. Non-limiting examples of RET inhibitor resistance mutations are described in Tables 3 and 4.

In some embodiments, dysregulation of a RET gene, a RET kinase, or the expression or activity or level of any of the same can be caused by an activating mutation in a RET gene (see, e.g., chromosome translocations that result in the expression of any of the fusion proteins listed in Table 1). In some embodiments, dysregulation of a RET gene, a RET kinase, or the expression or activity or level of any of the same can be caused by a genetic mutation that results in the expression of a RET kinase that has increased resistance to inhibition by a RET kinase inhibitor and/or a multi-kinase inhibitor (MKI), e.g., as compared to a wildtype RET kinase (see, e.g., the amino acid substitutions in Tables 3 and 4). The exemplary RET kinase point mutations, insertions, and deletions shown in Tables 2 and 2a can be caused by an activating mutation and/or can result in the expression of a RET kinase that has increased resistance to inhibition by a RET kinase inhibitor and/or a multi-kinase inhibitor (MKI).

The term “activating mutation” describes a mutation in a RET kinase gene that results in the expression of a RET kinase that has an increased kinase activity, e.g., as compared to a wildtype RET kinase, e.g., when assayed under identical conditions. For example, an activating mutation can result in the expression of a fusion protein that includes a RET kinase domain and a fusion partner. In another example, an activating mutation can be a mutation in a RET kinase gene that results in the expression of a RET kinase that has one or more (e.g., two, three, four, five, six, seven, eight, nine, or ten) amino acid substitutions (e.g., any combination of any of the amino acid substitutions described herein) that has increased kinase activity, e.g., as compared to a wildtype RET kinase, e.g., when assayed under identical conditions. In another example, an activating mutation can be a mutation in a RET kinase gene that results in the expression of a RET kinase that has one or more (e.g., two, three, four, five, six, seven, eight, nine, or ten) amino acids deleted, e.g., as compared to a wildtype RET kinase, e.g., when assayed under identical conditions. In another example, an activating mutation can be a mutation in a RET kinase gene that results in the expression of a RET kinase that has at least one (e.g., at least 2, at least 3, at least 4, at least 5, at least 6, at least 7, at least 8, at least 9, at least 10, at least 12, at least 14, at least 16, at least 18, or at least 20) amino acid inserted as compared to a wildtype RET kinase, e.g., the exemplary wildtype RET kinase described herein, e.g., when assayed under identical conditions. Additional examples of activating mutations are known in the art.

The term “wildtype” or “wild-type” describes a nucleic acid (e.g., a RET gene or a RET mRNA) or protein (e.g., a RET protein) that is found in a subject that does not have a RET-associated disease, e.g., a RET-associated cancer (and optionally also does not have an increased risk of developing a RET-associated disease and/or is not suspected of having a RET-associated disease), or is found in a cell or tissue from a subject that does not have a RET-associated disease, e.g., a RET-associated cancer (and optionally also does not have an increased risk of developing a RET-associated disease and/or is not suspected of having a RET-associated disease).

The term “regulatory agency” refers to a country's agency for the approval of the medical use of pharmaceutical agents with the country. For example, a non-limiting example of a regulatory agency is the U.S. Food and Drug Administration (FDA).

Provided herein is a method of treating cancer (e.g., a RET-associated cancer) in a patient in need of such treatment, the method comprising administering to the patient a therapeutically effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof or a pharmaceutical composition thereof. For example, provided herein are methods for treating a RET-associated cancer in a patient in need of such treatment, the method comprising a) detecting a dysregulation of a RET gene, a RET kinase, or the expression or activity or level of any of the same in a sample from the patient; and b) administering a therapeutically effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the dysregulation of a RET gene, a RET kinase, or the expression or activity or level of any of the same includes one or more fusion proteins. Non-limiting examples of RET gene fusion proteins are described in Table 1. In some embodiments, the fusion protein is KIF5B-RET. In some embodiments, the dysregulation of a RET gene, a RET kinase, or the expression or activity or level of any of the same includes one or more RET kinase protein point mutations/insertions. Non-limiting examples of RET kinase protein point mutations/insertions/deletions are described in Tables 2 and 2a. In some embodiments, the RET kinase protein point mutations/insertions/deletions are selected from the group consisting of M918T, M918V, C634W, V804L, and V804M. In some embodiments, a compound of Formula I is selected from i) Example No. 1-20; ii) Example No. 21-40; iii) Example No. 41-49; iv) Example No. 50-70; v) Example No. 71-90; vi) Example No. 91-110; vii) Example No. 111-121.

In some embodiments of any of the methods or uses described herein, the cancer (e.g., RET-associated cancer) is a hematological cancer. In some embodiments of any of the methods or uses described herein, the cancer (e.g., RET-associated cancer) is a solid tumor. In some embodiments of any of the methods or uses described herein, the cancer (e.g., RET-associated cancer) is a solid tumor. In some embodiments of any of the methods or uses described herein, the cancer (e.g., RET-associated cancer) is lung cancer (e.g., small cell lung carcinoma or non-small cell lung carcinoma), thyroid cancer (e.g., papillary thyroid cancer, medullary thyroid cancer, differentiated thyroid cancer, recurrent thyroid cancer, or refractory differentiated thyroid cancer), thyroid ademona, endocrine gland neoplasms, lung adenocarcinoma, bronchioles lung cell carcinoma, multiple endocrine neoplasia type 2A or 2B (MEN2A or MEN2B, respectively), pheochromocytoma, parathyroid hyperplasia, breast cancer, mammary cancer, mammary carcinoma, mammary neoplasm, colorectal cancer (e.g., metastatic colorectal cancer), papillary renal cell carcinoma, ganglioneuromatosis of the gastroenteric mucosa, inflammatory myofibroblastic tumor, or cervical cancer. In some embodiments of any of the methods or uses described herein, the cancer (e.g., RET-associated cancer) is selected from the group of: acute lymphoblastic leukemia (ALL), acute myeloid leukemia (AML), cancer in adolescents, adrenocortical carcinoma, anal cancer, appendix cancer, astrocytoma, atypical teratoid/rhabdoid tumor, basal cell carcinoma, bile duct cancer, bladder cancer, bone cancer, brain stem glioma, brain tumor, breast cancer, bronchial tumor, Burkitt lymphoma, carcinoid tumor, unknown primary carcinoma, cardiac tumors, cervical cancer, childhood cancers, chordoma, chronic lymphocytic leukemia (CLL), chronic myelogenous leukemia (CML), chronic myeloproliferative neoplasms, neoplasms by site, neoplasms, colon cancer, colorectal cancer, craniopharyngioma, cutaneous T-cell lymphoma, cutaneous angiosarcoma, bile duct cancer, ductal carcinoma in situ, embryonal tumors, endometrial cancer, ependymoma, esophageal cancer, esthesioneuroblastoma, Ewing sarcoma, extracranial germ cell tumor, extragonadal germ cell tumor, extrahepatic bile duct cancer, eye cancer, fallopian tube cancer, fibrous histiocytoma of bone, gallbladder cancer, gastric cancer, gastrointestinal carcinoid tumor, gastrointestinal stromal tumors (GIST), germ cell tumor, gestational trophoblastic disease, glioma, hairy cell tumor, hairy cell leukemia, head and neck cancer, thoracic neoplasms, head and neck neoplasms, CNS tumor, primary CNS tumor, heart cancer, hepatocellular cancer, histiocytosis, Hodgkin's lymphoma, hypopharyngeal cancer, intraocular melanoma, islet cell tumors, pancreatic neuroendocrine tumors, Kaposi sarcoma, kidney cancer, Langerhans cell histiocytosis, laryngeal cancer, leukemia, lip and oral cavity cancer, liver cancer, lung cancer, lymphoma, macroglobulinemia, malignant fibrous histiocytoma of bone, osteocarcinoma, melanoma, Merkel cell carcinoma, mesothelioma, metastatic squamous neck cancer, midline tract carcinoma, mouth cancer, multiple endocrine neoplasia syndromes, multiple myeloma, mycosis fungoides, myelodysplastic syndromes, myelodysplastic/myeloproliferative neoplasms, neoplasms by site, neoplasms, myelogenous leukemia, myeloid leukemia, multiple myeloma, myeloproliferative neoplasms, nasal cavity and paranasal sinus cancer, nasopharyngeal cancer, neuroblastoma, non-Hodgkin's lymphoma, non-small cell lung cancer, lung neoplasm, pulmonary cancer, pulmonary neoplasms, respiratory tract neoplasms, bronchogenic carcinoma, bronchial neoplasms, oral cancer, oral cavity cancer, lip cancer, oropharyngeal cancer, osteosarcoma, ovarian cancer, pancreatic cancer, papillomatosis, paraganglioma, paranasal sinus and nasal cavity cancer, parathyroid cancer, penile cancer, pharyngeal cancer, pheochromosytoma, pituitary cancer, plasma cell neoplasm, pleuropulmonary blastoma, pregnancy and breast cancer, primary central nervous system lymphoma, primary peritoneal cancer, prostate cancer, rectal cancer, colon cancer, colonic neoplasms, renal cell cancer, retinoblastoma, rhabdomyosarcoma, salivary gland cancer, sarcoma, Sezary syndrome, skin cancer, small cell lung cancer, small intestine cancer, soft tissue sarcoma, squamous cell carcinoma, squamous neck cancer, stomach cancer, T-cell lymphoma, testicular cancer, throat cancer, thymoma and thymic carcinoma, thyroid cancer, transitional cell cancer of the renal pelvis and ureter, unknown primary carcinoma, urethral cancer, uterine cancer, uterine sarcoma, vaginal cancer, vulvar cancer, and Wilms' tumor.

In some embodiments, a hematological cancer (e.g., hematological cancers that are RET-associated cancers) is selected from the group consisting of leukemias, lymphomas (non-Hodgkin's lymphoma), Hodgkin's disease (also called Hodgkin's lymphoma), and myeloma, for instance, acute lymphocytic leukemia (ALL), acute myeloid leukemia (AML), acute promyelocytic leukemia (APL), chronic lymphocytic leukemia (CLL), chronic myeloid leukemia (CML), chronic myelomonocytic leukemia (CMML), chronic neutrophilic leukemia (CNL), acute undifferentiated leukemia (AUL), anaplastic large-cell lymphoma (ALCL), prolymphocytic leukemia (PML), juvenile myelomonocyctic leukemia (JMML), adult T-cell ALL, AML with trilineage myelodysplasia (AML/TMDS), mixed lineage leukemia (MLL), myelodysplastic syndromes (MDSs), myeloproliferative disorders (MPD), and multiple myeloma (MM). Additional examples of hematological cancers include myeloproliferative disorders (MPD) such as polycythemia vera (PV), essential thrombocytopenia (ET) and idiopathic primary myelofibrosis (IMF/IPF/PMF). In one embodiment, the hematological cancer (e.g., the hematological cancer that is a RET-associated cancer) is AML or CMML.

In some embodiments, the cancer (e.g., the RET-associated cancer) is a solid tumor. Examples of solid tumors (e.g., solid tumors that are RET-associated cancers) include, for example, thyroid cancer (e.g., papillary thyroid carcinoma, medullary thyroid carcinoma), lung cancer (e.g., lung adenocarcinoma, small-cell lung carcinoma), pancreatic cancer, pancreatic ductal carcinoma, breast cancer, colon cancer, colorectal cancer, prostate cancer, renal cell carcinoma, head and neck tumors, neuroblastoma, and melanoma. See, for example, Nature Reviews Cancer, 2014, 14, 173-186.

In some embodiments, the cancer is selected from the group consisting of lung cancer, papillary thyroid cancer, medullary thyroid cancer, differentiated thyroid cancer, recurrent thyroid cancer, refractory differentiated thyroid cancer, multiple endocrine neoplasia type 2A or 2B (MEN2A or MEN2B, respectively), pheochromocytoma, parathyroid hyperplasia, breast cancer, colorectal cancer, papillary renal cell carcinoma, ganglioneuromatosis of the gastroenteric mucosa, and cervical cancer.

In some embodiments, the patient is a human.

Compounds of Formula I and pharmaceutically acceptable salts and solvates thereof are also useful for treating a RET-associated cancer.

Accordingly, also provided herein is a method for treating a patient diagnosed with or identified as having a RET-associated cancer, e.g., any of the exemplary RET-associated cancers disclosed herein, comprising administering to the patient a therapeutically effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof, or a pharmaceutical composition thereof as defined herein.

Dysregulation of a RET kinase, a RET gene, or the expression or activity or level of any (e.g., one or more) of the same can contribute to tumorigenesis. For example, a dysregulation of a RET kinase, a RET gene, or expression or activity or level of any of the same can be a translocation, overexpression, activation, amplification, or mutation of a RET kinase, a RET gene, or a RET kinase domain. Translocation can include a gene translocation resulting in the expression of a fusion protein that includes a RET kinase domain and a fusion partner. For example, a fusion protein can have increased kinase activity as compared to a wildtype RET protein. In some embodiments, a mutation in a RET gene can involve mutations in the RET ligand-binding site, extracellular domains, kinase domain, and in regions involved in protein:protein interactions and downstream signaling. In some embodiments, a mutation (e.g., an activating mutation) in a RET gene can result in the expression of a RET kinase having one or more (e.g., two, three, four, five, six, seven, eight, nine, or ten) amino acid substitutions (e.g., one or more amino acid substitutions in the kinase domain (e.g., amino acid positions 723 to 1012 in a wildtype RET protein), a gatekeeper amino acid (e.g., amino acid position 804 in a wildtype RET protein), the P-loop (e.g., amino acid positions 730-737 in a wildtype RET protein), the DFG motif (e.g., amino acid positions 892-894 in a wildtype RET protein), ATP cleft solvent front amino acids (e.g., amino acid positions 758, 811, and 892 in a wildtype RET protein), the activation loop (e.g., amino acid positions 891-916 in a wildtype RET protein), the C-helix and loop preceeding the C-helix (e.g., amino acid positions 768-788 in a wildtype RET protein), and/or the ATP binding site (e.g., amino acid positions 730-733, 738, 756, 758, 804, 805, 807, 811, 881, and 892 in a wildtype RET protein). In some embodiments, a mutation can be a gene amplification of a RET gene. In some embodiments, a mutation (e.g., an activating mutation) in a RET gene can result in the expression of a RET kinase that lacks at least one amino acid (e.g., at least 2, at least 3, at least 4, at least 5, at least 6, at least 7, at least 8, at least 9, at least 10, at least 12, at least 14, at least 16, at least 18, at least 20, at least 25, at least 30, at least 35, at least 40, at least 45, or at least 50 amino acids) as compared to a wildtype RET protein. In some embodiments, dyregulation of a RET kinase can be increased expression (e.g., increased levels) of a wildtype RET kinase in a mammalian cell due to aberrant cell signaling and/or dysregulated autocrine/paracrine signaling (e.g., as compared to a control non-cancerous cell). In some embodiments, a mutation (e.g., an activating mutation) in a RET gene can result in the expression of a RET kinase that has at least one amino acid (e.g., at least 2, at least 3, at least 4, at least 5, at least 6, at least 7, at least 8, at least 9, at least 10, at least 12, at least 14, at least 16, at least 18, at least 20, at least 25, at least 30, at least 35, at least 40, at least 45, or at least 50 amino acids) inserted as compared to a wildtype RET protein. In some embodiments, dyregulation of a RET kinase can be increased expression (e.g., increased levels) of a wildtype RET kinase in a mammalian cell (e.g., as compared to a control non-cancerous cell), e.g., due to aberrant cell signaling and/or dysregulated autocrine/paracrine signaling. Other dysregulations can include RET mRNA splice variants. In some embodiments, the wildtype RET protein is the exemplary wildtype RET protein described herein.

In some embodiments, the dysregulation of a RET gene, a RET kinase, or expression or activity or level of any of the same, includes overexpression of wild-type RET kinase (e.g., leading to autocrine activation). In some embodiments, the dysregulation of a RET gene, a RET kinase protein, or expression or activity or level of any of the same, includes overexpression, activation, amplification, or mutation in a chromosomal segment comprising the RET gene or a portion thereof, including, for example, the kinase domain portion, or a portion capable of exhibiting kinase activity.

In some embodiments, the dysregulation of a RET gene, a RET kinase protein, or expression or activity or level of any of the same, includes one or more chromosome translocations or inversions resulting in a RET gene fusion. In some embodiments, the dysregulation of a RET gene, a RET kinase protein, or expression or activity or level of any of the same, is a result of genetic translocations in which the expressed protein is a fusion protein containing residues from a non-RET partner protein, and includes a minimum of a functional RET kinase domain.

Non-limiting examples of RET fusion proteins are shown in Table 1.

TABLE 1 Exemplary RET Fusion Partners and Cancers Non-limiting Exemplary Fusion Partner RET-Associated Cancer(s) BCR Chronic Myelomonocytic Leukemia (CMML) CLIP1 Adenocarcinoma KIF5B NSCLC, Ovarian Cancer, Spitzoid Neoplasms; Lung Adenocarcinoma^(3, 4,14, 28); Adenosquamous Carcinomas¹⁵ CCDC6 (also NSCLC, Colon Cancer, called PTC1, Papillary Thyroid Cancer; D10S170, or H4) Adenocarcinomas; Lung Adenocarcinoma; Metastatic Colorectal Cancer⁵; Adenosquamous Carcinomas¹⁵, Breast Cancer³⁰ PTC1ex9 (a novel Metastatic papillary thyroid CCDC6 cancer² rearrangement) NCOA4 (also Papillary Thyroid Cancer²¹, called PTC3, NSCLC, Colon Cancer, ELE1, and RFG) Salivary Gland Cancer, Metastatic Colorectal Cancer⁵; Lung Adenocarcinoma¹⁵; Adenosquamous Carcinomas¹⁵ Diffuse Sclerosing Variant of Papillary Thyroid Cancer¹⁶, Breast Cancer³⁰, Acinic Cell Carcinoma³², Mammary Analog Secretory Carcinoma³³ TRIM33 (also NSCLC, Papillary Thyroid called PTC7 and Cancer RFG7) ERC1 (also called Papillary Thyroid Cancer, ELKS) Breast Cancer FGFR1OP CMML, Primary Myelofibrosis with secondary Acute Myeloid Leukemia MBD1(also known Papillary Thyroid Cancer as PCM1) RAB61P2 Papillary Thyroid Cancer PRKAR1A (also Papillary Thyroid Cancer called PTC2) TRIM24 (also Papillary Thyroid Cancer called PTC6) KTN1 (also called Papillary Thyroid Cancer PTC8 ) GOLGA5 (also Papillary Thyroid Cancer, called PTC5) Spitzoid Neoplasms HOOK3 Papillary Thyroid Cancer KIAA1468 (also Papillary Thyroid Cancer, called PTC9 and Lung Adenocarcinoma^(8, 12) RFG9) TRIM27 (also Papillary Thyroid Cancer called RFP) AKAP13 Papillary Thyroid Cancer FKBP15 Papillary Thyroid Cancer SPECC1L Papillary Thyroid Cancer; Thyroid Gland Carcinoma TBL1XR1 Papillary Thyroid Cancer; Thyroid Gland Carcinoma CEP55 Diffuse Gastric Cancer⁷ CUX1 Lung Adenocarcinoma ACBD5 Papillary Thyroid Carcinoma MYH13 Medullary Thyroid Carcinoma¹ Uncharacterized Inflammatory Myofibroblastic Tumor⁶ PIBF1 Bronchiolus Lung Cell Carcinoma⁹ KIAA1217 (also Papillary Thyroid Cancer^(10, 13) called SKT) Lung Adenocarcinoma¹⁴ NSCLC¹⁴ MPRIP NSCLC¹¹ HRH4-RET Thyroid Cancer and/or Paillary Thyroid Carcinoma¹⁷ Ria-RET Thyroid Cancer and/or Papillary Thyroid Carcinoma¹⁷ RFG8 Papillary Thyroid Carcinoma¹⁸ FOXP4 Lung Adenocarcinoma¹⁹ MYH10 Infantile Myofibromatosis²⁰ HTIF1 Various²² TIF1G Various²² H4L Various²² PTC4 (a novel Papillary Thyroid Cancer²³ NCO4/ELE1 rearrangement) FRMD4A NSCLC²⁴ SQSTM1 Papillary Thyroid Carcinoma²⁵ AFAP1L2 Papillary Thyroid Carcinoma²⁵ AFAP1 NSCLC³¹ PPFIBP2 Papillary Thyroid Carcinoma²⁵ EML4 Papillary Thyroid Cancer²⁶ PARD3 NSCLC²⁷ UVELD Papillary Thyroid Cancer²⁹ RASGEF1A Breast Cancer³⁰ TEL In vitro³⁴ RUFY1 Colorectal Cancer³⁵ OLFM4 Small-Bowel Cancer³⁶ UEVLD Papillary Thyroid Carcinoma²⁹ DLG5 Non-Anaplastic Thyroid (NAT) Cancer³⁷ RRBP1 Colon Cancer³⁸ ETV6 Secretory Carcinoma³⁹ ¹Grubbs et al., J. Clin. Endocrinol. Metab. 100: 788-793, 2015. ²Halkova et al., Human Pathology 46: 1962-1969, 2015. ³U.S. Pat. No. 9,297,011 ⁴ U.S. Pat. No. 9,216,172 ⁵Le Rolle et al., Oncotarget. 6(30): 28929-37, 2015. ⁶Antonescu et al., Am J Surg Pathol. 39(7): 957-67, 2015. ⁷U.S. Patent Application Publication No. 2015/0177246. ⁸U.S. Patent Application Publication No. 2015/0057335. ⁹Japanese Patent Application Publication No. 2015/109806A. ¹⁰Chinese Patent Application Publication No. 105255927A. ¹¹Fang, et al. Journal of Thoracic Oncology 11.2 (2016): S21-S22. ¹² European Patent Application Publication No. EP3037547A1. ¹³ Lee et al., Oncotarget. DOI: 10.18632/oncotarget.9137, e-published ahead of printing, 2016. ¹⁴Saito et al., Cancer Science 107: 713-720, 2016. ¹⁵Pirker et al., Transl. Lung Cancer Res. 4(6): 797-800, 2015. ¹⁶Joung et al., Histopathology 69(1): 45-53, 2016. ¹⁷PCT Patent Application Publication No. WO 2016/141169. ¹⁸Klugbauer et al., Cancer Res., 60(24): 7028-32, 2000. ¹⁹Bastien et al., Journal of Molecular Diagnostics, 18(6): 1027, Abstract Number: S120, 2016 Annual Meeting of the Association for Molecular Pathology, Charlotte, NC, 2016. ²⁰Rosenzweig et al., Pediatr Blood Cancer, doi: 10.1002/pbc.26377, 2016. ²¹Su et al., PLoS One, 11(111): e0165596, 2016. ²²U.S. Pat. No. 9,487,491. ²³Fugazzola et al., Oncogene, 13(5): 1093-7, 1996. ²⁴Velcheti et al., J Thorac Oncol., 12(2): e15-e16. doi: 10.1016/j.jtho.2016.11.274, 2017. ²⁵Iyama et al., Thyroid, doi: 10.1089/thy.2016.0673, 2017. ²⁶Demeure et al., World J Surg. 38(6): 1296-305. doi: 10.1007/s00268-014-2485-3, 2014. ²⁷Sabari et al., Oncoscience, Advance Publications, www.impactjournals.com/oncoscience/files/papers/1/345/345.pdf, 2017. ²⁸ U.S. Patent Application Publication No. 2017/0014413. ²⁹Lu et al., Oncotarget, 8(28): 45784-45792, doi: 10.18632/oncotarget.17412, 2017. ³⁰Hirshfield et al., Cancer Research, (February 2017) Vol. 77, No. 4, Supp. 1. Abstract Number: P3-07-02. Meeting Info: 39th Annual CTRC-AACR San Antonio Breast Cancer Symposium. San Antonio, TX, United States. 6 Dec. 2016-10 Dec. 2016. ³¹Morgensztern et al., Journal of Thoracic Oncology, (January 2017) Vol. 12, No. 1, Supp. 1, pp. S717-S718, Abstract Number: P1.07-035, Meeting Info: 17th World Conference of the International Association for the Study of Lung Cancer, IASLC 2016. Vienna, Austria. 4 Dec. 2016. ³²Dogan et al., Laboratory Investigation, (February 2017) Vol. 97, Supp. 1, pp. 323A. Abstract Number: 1298, Meeting Info: 106th Annual Meeting of the United States and Canadian Academy of Pathology, USCAP 2017. San Antonio, TX, United States. ³³Dogan et al., MODERN PATHOLOGY, Vol. 30, Supp. [2], pp. 323A-323A. MA 1298, 2017. ³⁴PCT Patent Application Publication No. WO 2017/146116. ³⁵PCT Patent Application Publication No. WO 2017/122815. ³⁶Reeser et al., J. Mol. Diagn., 19(5): 682-696, doi: 10.1016/j.jmoldx.2017.05.006, 2017. ³⁷Ibrahimpasic et al., Clin. Cancer Res., doi: 10.1158/1078-0432.CCR-17-1183, 2017. ³⁸Kloosterman et al., Cancer Res., 77(14): 3814-3822. doi: 10.1158/0008-5472.CAN-16-3563, 2017. ³⁹Skalova et al., Am. J. Surg. Pathol., 42(2): 234-246 (2018). doi: 10.1097/PAS.0000000000000972

In some embodiments, the dysregulation of a RET gene, a RET kinase, or expression or activity or level of any of the same, includes one or more deletions (e.g., deletion of an amino acid at position 4), insertions, or point mutation(s) in a RET kinase. In some embodiments, the dysregulation of a RET gene, a RET kinase, or expression or activity or level of any of the same, includes a deletion of one or more residues from the RET kinase, resulting in constitutive activity of the RET kinase domain.

In some embodiments, the dysregulation of a RET gene, a RET kinase, or expression or activity or level of any of the same, includes at least one point mutation in a RET gene that results in the production of a RET kinase that has one or more amino acid substitutions, insertions, or deletions as compared to the wild-type RET kinase (see, for example, the point mutations listed in Table 2).

TABLE 2 Activating RET Kinase Protein Amino Acid Substitutions/Insertions/Deletions Exemplary RET Amino Acid Substitutions^(A) Amino acid position 2 Amino acid position 3 Amino acid position 4 Amino acid position 5 Amino acid position 6 Amino acid position 7 Amino acid position 8 Amino acid position 11 Amino acid position 12 Amino acid position 13 Amino acid position 20 Amino acid position 32 (e.g., S32L) Amino acid position 34 (e.g., D34S) Amino acid position 40 (e.g., L40P) Amino acid position 56 (e.g., L56M)³⁰ Amino acid position 64 (e.g., P64L) Amino acid position 67 (e.g., R67H) Amino acid position 114 (e.g., R114H) Amino acid position 136 (e.g., glutamic acid to stop codon) Amino acid position 145 (e.g., V145G) Amino acid position 180 (e.g., arginine to stop codon) Amino acid position 200 Amino acid position 292 (e.g., V292M) Amino acid position 294 Amino acid position 321 (e.g., G321R) Amino acid position 330 (e.g., R330Q) Amino acid position 338 (e.g., T338I) Amino acid position 360 (e.g., R360W) Amino acid position 373 (e.g., alanine to frameshift) Amino acid position 393 (e.g., F393L) Amino acid position 423 (e.g., G423R)²⁷ Amino acid position 432 Amino acid position 446 (e.g., G446R)²⁸ Δ Amino acid residues 505-506 (6-Base Pair In-Frame Germline Deletion in Exon 7)³ Amino acid position 510 (e.g., A510V) Amino acid position 511 (e.g., E511K) Amino acid position 513 (e.g., G513D)⁷* Amino acid position 515 (e.g., C515S, C515W⁴) Amino acid position 525 (e.g., R525W)⁷* Amino acid position 531 (e.g., C531R, or 9 base pair duplication²) Amino acid position 532 (e.g., duplication)² Amino acid position 533 (e.g., G533C, G533S) Amino acid position 550 (e.g., G550E) Amino acid position 591 (e.g., V591I) Amino acid position 593 (e.g., G593E) Amino acid position 595 (e.g., E595D and E595A)¹⁸ Amino acid position 600 (e.g., R600Q) Amino acid position 602 (e.g., I602V)⁶ Amino acid position 603 (e.g., K603Q, K603E²) Amino acid position 606 (e.g., Y606C) Amino acid position 609 (e.g., C609Y, C609S, C609G, C609R, C609F, C609W, C690C³²) Amino acid position 611 (e.g., C611R, C611S, C611G, C611Y, C611F, C611W) Amino acid position 616 (e.g., E616Q)²³ Amino acid position 618 (e.g., C618S, C618Y, C618R, C618Y, C618G, C618F, C618W) Amino acid position 619 (e.g., F619F) Amino acid position 620 (e.g., C620S, C620W, C620R, C620G, C620L, C620Y, C620F) Amino acid position 623 (e.g., E623K) Amino acid position 624 (e.g., D624N) Amino acid position 630 (e.g., C630A, C630R, C630S, C630Y, C630F, C630W) Amino acid position 631 (e.g., D631N, D631Y, D631A, D631G, D631V, D631E,) Amino acid position 632 (e.g., E632K, E632G^(5, 11)) Δ Amino acid residues 632-633 (6-Base Pair In-Frame Germline Deletion in Exon 11)⁹ Amino acid position 633 (e.g., 9 base pair duplication²) Amino acid position 634 (e.g., C634W, C634Y, C634S, C634R, C634F, C634G, C634L, C634A, or C634T, or an insertion ELCR², or a 12 base pair duplication²) (e.g., causing MTC) Amino acid position 635 (e.g., R635G) Amino acid position 636 (e.g., T636P², T636M⁴) Amino acid position 640 (e.g., A640G) Amino acid position 641 (e.g., A641S, A641T⁸) Amino acid position 648 (e.g., V648I) Amino acid position 649 (e.g., S649L)²⁸ Amino acid position 664 (e.g., A664D) Amino acid position 665 (e.g., H665Q) Amino acid position 666 (e.g., K666E, K666M, K666N, K666R) Amino acid position 675 (T675T, silent nucleotide change)¹⁸ Amino acid position 686 (e.g., S686N) Amino acid position 689 (e.g., S689T)¹⁸ Amino acid position 691 (e.g., G691S) Amino acid position 694 (e.g., R694Q) Amino acid position 700 (e.g., M700L) Amino acid position 706 (e.g., V706M, V706A) Amino acid position 713 splice variant (e.g., E713K)⁶ Amino acid position 732 (e.g., E732K)²⁰ Amino acid position 736 (e.g., G736R)⁶ Amino acid position 748 (e.g., G748C) Amino acid position 750 (e.g., A750P) Amino acid position 765 (e.g., S765P) Amino acid position 766 (e.g., P766S, P766M⁶) Amino acid position 768 (e.g., E768Q, E768D) Amino acid position 769 (e.g., L769L) Amino acid position 770 (e.g., R770Q) Amino acid position 771 (e.g., D771N) Amino acid position 777 (e.g., N777S) Amino acid position 778 (e.g., V778I) Amino acid position 781 (e.g., Q781R) Amino acid position 788 (e.g., I788I³²) Amino acid position 790 (e.g., L790F) Amino acid position 791 (e.g., Y791F, Y791N²⁴) Amino acid position 802 Amino acid position 804 (e.g., V804L^(15, 16), V804M^(15, 16), V804E¹²) (e.g., causing MTC) Amino acid position 805 (e.g., E805K) Amino acid position 804/805 (e.g., V804M/E805K)¹⁷ Amino acid position 806 (e.g., Y806F, Y806S¹², Y806G, Y806C^(2,12,14), Y806E¹⁴, Y806H¹², Y806N^(12,) Y806Y³²) Amino acid position 810 (e.g., G810R¹², G810S¹², G810A¹³) Amino acid position 818 (e.g., E818K) Amino acid position 819 (e.g., S819I) Amino acid position 823 (e.g., G823E) Amino acid position 826 (e.g., Y826M, Y826S)¹⁰ Amino acid position 833 (e.g., R833C) Amino acid position 836 (e.g., S836S)¹⁹ Amino acid position 841 (e.g., P841L, P841P) Amino acid position 843 (e.g., E843D) Amino acid position 844 (e.g., R844W, R844Q, R844L) Amino acid position 848 (e.g., M848T) Amino acid position 852 (e.g., I852M) Amino acid position 865 (e.g., L865V)¹² Amino acid position 866 (e.g., A866W)³³ Amino acid position 870 (e.g., L870F)¹² Amino acid position 873 (e.g., R873W) Amino acid position 876 (e.g., A876V) Amino acid position 881 (e.g., L881V) Amino acid position 882 Amino acid position 883 (e.g., A883F, A883S, A883T) Amino acid position 884 (e.g., E884K) Amino acid position 886 (e.g., R886W) Amino acid position 891 (e.g., S891A, S891S³²) Amino acid position 897 (e.g., R897Q) Amino acid position 898 (e.g., D898V) Amino acid position 900 (e.g., Y900F)²² Amino acid position 901 (e.g., E901K) Amino acid position 904 (e.g., S904F, S904S, S904C²) Amino acid position 905 (e.g., Y905F)²² Amino acid position 907 (e.g., K907E, K907M) Amino acid position 908 (e.g., R908K) Amino acid position 911 (e.g., G911D) Amino acid position 912 (e.g., R912P, R912Q) Amino acid position 918 (e.g., M918T², M918V, M918L⁶) (e.g., causing MTC) Amino acid position 919 (e.g., A919V) Amino acid position 921 (e.g., E921K) Amino acid position 922 (e.g., S922P, S922Y) Amino acid position 930 (e.g., T930M) Amino acid position 961 (e.g., F961L) Amino acid position 972 (e.g., R972G) Amino acid position 981 (e.g., Y981F)²² Amino acid position 982 (e.g., R982C) Amino acid position 1009 (e.g., M1009V) Amino acid position 1015 (e.g., Y1015F)²² Amino acid position 1017 (e.g., D1017N) Amino acid position 1041 (e.g., V1041G) Amino acid position 1064 (e.g., M1064T) Amino acid position 1096 (e.g., Y1096F)²¹ Amino acid position 1109 (e.g., M1109T)³⁴ RET + 3¹ (In-Frame Deletion in Exons 6 and 11)²⁵ (3 bp In-Frame Deletion in Exon 15)²⁶ Nucleotide position 2136 + 2 (e.g., 2136 + 2T > G)²⁹ (del632-636 ins6)³¹ Amino acid positions 791 and 852 (e.g., Y791F + I852M)³¹ Amino acid positions 634 and 852 (e.g., C634R + I852M)³¹ ^(A)The RET kinase mutations shown may be activating mutations and/or confer increased resistance of the RET kinase to a RET kinase inhibitor and/or a multi-kinase inhibitor (MKI), e.g., as compared to a wildtype RET kinase. ¹U.S. Patent Application Publication No. 2014/0272951. ²Krampitz et al., Cancer 120: 1920-1931, 2014. ³Latteyer, et al., J. Clin. Endocrinol. Metab. 101(3): 1016-22, 2016. ⁴Silva, et al. Endocrine 49.2: 366-372, 2015. ⁵Scollo, et al., Endocr. J. 63(1): 87-91, 2016. ⁶Jovanovic, et al., Prilozi 36(1): 93-107, 2015. ⁷Qi, et al., Oncotarget. 6(32): 33993-4003, 2015. *R525W and G513D appear to act in combination with S891A to enchance oncogenic activity. ⁸Kim, et al. ACTA ENDOCRINOLOGICA-BUCHAREST 11.2, 189-194, 2015. ⁹Cecchirini, et al. Oncogene, 14, 2609-2612, 1997. ¹⁰Karrasch, et al. Eur. Thyroid J. 5(1): 73-7, 2016. ¹¹ Scollo et al., Endocr. J. 63: 87-91, 2016. ¹²PCT Patent Application Publication No. WO 2016/127074. ¹³Huang et al., Mol. Cancer Ther., 2016 Aug. 5. pii: molcanther.0258.2016. [Epub ahead of print]. ¹⁴Carlomagno, et al., Endocr. Rel. Cancer 16(1): 233-41, 2009. ¹⁵Yoon et al., J. Med. Chem. 59(1): 358-73, 2016. ¹⁶ U.S. Pat. No. 8,629,135. ¹⁷Cranston, et al., Cancer Res. 66(20): 10179-87, 2006. ¹⁸Kheiroddin et al., Clin. Lab. 62(5): 871-6, 2016. ¹⁹Ceolin et al., PLoS One. 11(2): e0147840, doi: 10.1371/journal.pone.0147840, 2016. ²⁰Mamedova et al., Summer Undergraduate Research Programs (SURP) Student Abstracts, University of Oklahoma Health Sciences Center, 2016. ²¹Liu et al., J. Biol. Chem., 271(10): 5309-12, 1995. ²²Kato et al., Cancer Res., 62: 2414-22, 2002. ²³Grey et al., Endocrine Pathology, doi: 10.1007/s12022-016-9451-6, 2016. ²⁴De Almeida et al., Endocrine Reviews, 2016, Vol. 37, No. 2, Supp. Supplement 1. Abstract Number: SUN-068; 98^(th) Annual Meeting and Expo of the Endocrine Society, ENDO 2016. Boston, MA, US. 1 Apr. 2016-4 Apr. 2016. ²⁵Vanden et al., Annals of Oncology, 2016, Vol. 27, Supp. Supplement 6. Abstract Number: 427PD; 41^(st) European Society for Medical Oncology Congress, ESMP 2016. Copenhagen, Denmark. 7 Oct. 2016-11 Oct. 2016. ²⁶Romei et al., European Thyroid Journal (August 2016) Vol. 5, Supp. Supplement 1, pp. 75; 39th Annual Meeting of the European Thyroid Association, ETA 2016. Copenhagen, Denmark. 3 Sep. 2016-6 Sep. 2016. ²⁷Lee et al., Oncotarget, 8(4): 6579-6588, doi: 10.18632/oncotarget.14172, 2017. ²⁸Zhang et al., Laboratory Investigation, (February 2017) Vol. 97, Supp. 1, pp. 209A. Abstract Number: 840, Meeting Info: 106th Annual Meeting of the United States and Canadian Academy of Pathology, USCAP 2017. San Antonio, TX, United States. ²⁹Borecka et al., European Journal of Cancer, (July 2016) Vol. 61, No. 1, pp. S26, Abstract Number: 162, Meeting Info: 24th Biennial Congress of the European Association for Cancer Research, EACR 2016. Manchester, United Kingdom. ³⁰Corsello et al., Endocrine Reviews, (JUNE 2014) Vol. 35, No. 3, Suppl. S, pp. SUN-0322, Meeting Info.: 96th Annual Meeting and Expo of the Endocrine-Society, Chicago, IL, USA, Jun. 21-24, 2014. ³¹Gazizova et al., Endocrine Reviews, (JUNE 2014) Vol. 35, No. 3, Suppl. S, pp. SAT-0304, Meeting Info.: 96th Annual Meeting and Expo of the Endocrine-Society, Chicago, IL, USA, Jun. 21-24, 2014. ³²Sromek et al., Endocr Pathol., doi: 10.1007/s12022-017-9487-2, 2017. ³³U.S. Patent Application Publication No. 2017/0267661. ³⁴Davila et. al., Rare Tumors, 2017; 9(2): 6834. doi: 10.4081/rt.2017.6834.

In some embodiments, the dysregulation of a RET gene, a RET kinase, or expression or activity or level of any of the same, includes at least one point mutation in a RET gene that results in the production of a RET kinase that has one or more amino acid substitutions, insertions, or deletions as compared to the wild-type RET kinase (see, for example, the point mutations listed in Table 2a).

TABLE 2a Exemplary RET Kinase Protein Point Mutations/Insertions/Deletions Exemplary RET Point Mutations^(A) Amino acid position 20 Amino acid position 32 (e.g., S32L) Amino acid position 34 (e.g., D34S) Amino acid position 40 (e.g., L40P) Amino acid position 64 (e.g., P64L) Amino acid position 67 (e.g., R67H) Amino acid position 114 (e.g., R114H) Amino acid position 145 (e.g., V145G) Amino acid position 200 Amino acid position 292 (e.g., V292M) Amino acid position 294 Amino acid position 321 (e.g., G321R) Amino acid position 330 (e.g., R330Q) Amino acid position 338 (e.g., T338I) Amino acid position 360 (e.g., R360W) Amino acid position 393 (e.g., F393L) Amino acid position 432 Δ Amino acid residues 505-506 (6-Base Pair In-Frame Germline Deletion in Exon 7) Amino acid position 510 (e.g., A510V) Amino acid position 511 (e.g., E511K) Amino acid position 513 (e.g., G513D) Amino acid position 515 (e.g., C515S, C515W⁴) Amino acid position 525 (e.g., R525W) Amino acid position 531 (e.g., C531R, or 9 base pair duplication) Amino acid position 532 (e.g., duplication) Amino acid position 533 (e.g., G533C, G533S) Amino acid position 550 (e.g., G550E) Amino acid position 591 (e.g., V591I) Amino acid position 593 (e.g., G593E) Amino acid position 595 (e.g., E595D and E595A) Amino acid position 600 (e.g., R600Q) Amino acid position 602 (e.g., I602V) Amino acid position 603 (e.g., K603Q, K603E) Amino acid position 606 (e.g., Y606C) Amino acid position 609 (e.g., C609Y, C609S, C609G, C609R, C609F, C609W) Amino acid position 611 (e.g., C611R, C611S, C611G, C611Y, C611F, C611W) Amino acid position 616 (e.g., E616Q) Amino acid position 618 (e.g., C618S, C618Y, C618R, C618G, C618F, C618W) Amino acid position 620 (e.g., C620S, C620W, C620R, C620G, C620L, C620Y, C620F) Amino acid position 623 (e.g., E623K) Amino acid position 624 (e.g., D624N) Amino acid position 630 (e.g., C630A, C630R, C630S, C630Y, C630F, C630W) Amino acid position 631 (e.g., D631N, D631Y, D631A, D631G, D631V, D631E,) Amino acid position 632 (e.g., E632K, E632G) Δ Amino acid residues 632-633 (6-Base Pair In-Frame Germline Deletion in Exon 11) Amino acid position 633 (e.g., 9 base pair duplication) Amino acid position 634 (e.g., C634W, C634Y, C634S, C634R, C634F, C634G, C634L, C634A, or C634T, or an insertion ELCR, or a 12 base pair duplication) (e.g., causing MTC) Amino acid position 635 (e.g., R635G) Amino acid position 636 (e.g., T636P, T636M) Amino acid position 640 (e.g., A640G) Amino acid position 641 (e.g., A641S, A641T) Amino acid position 648 (e.g., V648I) Amino acid position 649 (e.g., S649L) Amino acid position 664 (e.g., A664D) Amino acid position 665 (e.g., H665Q) Amino acid position 666 (e.g., K666E, K666M, K666N, K666R) Amino acid position 686 (e.g., S686N) Amino acid position 689 (e.g., S689T) Amino acid position 691 (e.g., G691S) Amino acid position 694 (e.g., R694Q) Amino acid position 700 (e.g., M700L) Amino acid position 706 (e.g., V706M, V706A) Amino acid position 713 splice variant (e.g., E713K) Amino acid position 732 (e.g., E732K) Amino acid position 736 (e.g., G736R) Amino acid position 748 (e.g., G748C) Amino acid position 750 (e.g., A750P) Amino acid position 765 (e.g., S765P) Amino acid position 766 (e.g., P766S, P766M) Amino acid position 768 (e.g., E768Q, E768D) Amino acid position 769 (e.g., L769L) Amino acid position 770 (e.g., R770Q) Amino acid position 771 (e.g., D771N) Amino acid position 777 (e.g., N777S) Amino acid position 778 (e.g., V778I) Amino acid position 781 (e.g., Q781R) Amino acid position 790 (e.g., L790F) Amino acid position 791 (e.g., Y791F, Y791N) Amino acid position 802 Amino acid position 804 (e.g., V804L, V804M, V804E) (e.g., causing MTC) Amino acid position 805 (e.g., E805K) Amino acid position 804/805 (e.g., V804M/E805K) Amino acid position 806 (e.g., Y806F, Y806S, Y806G, Y806C, Y806E, Y806H, Y806N) Amino acid position 810 (e.g., G810R, G810S, G810A) Amino acid position 818 (e.g., E818K) Amino acid position 819 (e.g., S819I) Amino acid position 823 (e.g., G823E) Amino acid position 826 (e.g., Y826M, Y826S) Amino acid position 833 (e.g., R833C) Amino acid position 836 (e.g., S836S) Amino acid position 841 (e.g., P841L, P841P) Amino acid position 843 (e.g., E843D) Amino acid position 844 (e.g., R844W, R844Q, R844L) Amino acid position 848 (e.g., M848T) Amino acid position 852 (e.g., I852M) Amino acid position 865 (e.g., L865V) Amino acid position 870 (e.g., L870F) Amino acid position 873 (e.g., R873W) Amino acid position 876 (e.g., A876V) Amino acid position 881 (e.g., L881V) Amino acid position 882 Amino acid position 883 (e.g., A883F, A883S, A883T) Amino acid position 884 (e.g., E884K) Amino acid position 886 (e.g., R886W) Amino acid position 891 (e.g., S891A) Amino acid position 897 (e.g., R897Q) Amino acid position 898 (e.g., D898V) Amino acid position 900 (e.g., Y900F) Amino acid position 901 (e.g., E901K) Amino acid position 904 (e.g., S904F, S904S, S904C) Amino acid position 907 (e.g., K907E, K907M) Amino acid position 908 (e.g., R908K) Amino acid position 911 (e.g., G911D) Amino acid position 912 (e.g., R912P, R912Q) Amino acid position 918 (e.g., M918T, M918V, M918L) (e.g., causing MTC) Amino acid position 919 (e.g., A919V) Amino acid position 921 (e.g., E921K) Amino acid position 922 (e.g., S922P, S922Y) Amino acid position 930 (e.g., T930M) Amino acid position 961 (e.g., F961L) Amino acid position 972 (e.g., R972G) Amino acid position 982 (e.g., R982C) Amino acid position 1009 (e.g., M1009V) Amino acid position 1015 (e.g., Y1015F) Amino acid position 1017 (e.g., D1017N) Amino acid position 1041 (e.g., V1041G) Amino acid position 1064 (e.g., M1064T) Amino acid position 1096 (e.g., Y1096F) RET + 3 (In-Frame Deletion in Exons 6 and 11) (3bp In-Frame Deletion in Exon 15) ^(A)The RET kinase mutations shown above may be activating mutations and/or may confer increased resistance of the RET kinase to a RET inhibitor and/or a multi-kinase inhibitor (MKI), e.g., as compared to a wildtype RET kinase.

In some embodiments, the dysregulation of a RET gene, a RET kinase, or expression or activity or level of any of the same, includes a splice variation in a RET mRNA which results in an expressed protein that is an alternatively spliced variant of RET having at least one residue deleted (as compared to the wild-type RET kinase) resulting in a constitutive activity of a RET kinase domain.

A “RET kinase inhibitor” as defined herein includes any compound exhibiting RET inhibition activity. In some embodiments, a RET kinase inhibitor is selective for a RET kinase. Exemplary RET kinase inhibitors can exhibit inhibition activity (IC₅₀) against a RET kinase of less than about 1000 nM, less than about 500 nM, less than about 200 nM, less than about 100 nM, less than about 50 nM, less than about 25 nM, less than about 10 nM, or less than about 1 nM as measured in an assay as described herein. In some embodiments, a RET kinase inhibitor can exhibit inhibition activity (IC₅₀) against a RET kinase of less than about 25 nM, less than about 10 nM, less than about 5 nM, or less than about 1 nM as measured in an assay as provided herein.

As used herein, a “first RET kinase inhibitor” or “first RET inhibitor” is a RET kinase inhibitor as defined herein, but which does not include a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof as defined herein. As used herein, a “second RET kinase inhibitor” or a “second RET inhibitor” is a RET kinase inhibitor as defined herein, but which does not include a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof as defined herein. When both a first and a second RET inhibitor are present in a method provided herein, the first and second RET kinase inhibitor are different.

In some embodiments, the dysregulation of a RET gene, a RET kinase, or expression or activity or level of any of the same, includes at least one point mutation in a RET gene that results in the production of a RET kinase that has one or more amino acid substitutions or insertions or deletions in a RET gene that results in the production of a RET kinase that has one or more amino acids inserted or removed, as compared to the wild-type RET kinase. In some cases, the resulting RET kinase is more resistant to inhibition of its phosphotransferase activity by one or more first RET kinase inhibitor(s), as compared to a wildtype RET kinase or a RET kinase not including the same mutation. Such mutations, optionally, do not decrease the sensitivity of the cancer cell or tumor having the RET kinase to treatment with a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof (e.g., as compared to a cancer cell or a tumor that does not include the particular RET inhibitor resistance mutation). In such embodiments, a RET inhibitor resistance mutation can result in a RET kinase that has one or more of an increased V_(max), a decreased K_(m) for ATP, and an increased K_(D) for a first RET kinase inhibitor, when in the presence of a first RET kinase inhibitor, as compared to a wildtype RET kinase or a RET kinase not having the same mutation in the presence of the same first RET kinase inhibitor.

In other embodiments, the dysregulation of a RET gene, a RET kinase, or expression or activity or level of any of the same, includes at least one point mutation in a RET gene that results in the production of a RET kinase that has one or more amino acid substitutions as compared to the wild-type RET kinase, and which has increased resistance to a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof, as compared to a wildtype RET kinase or a RET kinase not including the same mutation. In such embodiments, a RET inhibitor resistance mutation can result in a RET kinase that has one or more of an increased V_(max), a decreased K_(m), and a decreased K_(D) in the presence of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof, as compared to a wildtype RET kinase or a RET kinase not having the same mutation in the presence of the same compound of Formula I or a pharmaceutically acceptable salt or solvate thereof.

Examples of RET inhibitor resistance mutations can, e.g., include point mutations, insertions, or deletions in and near the ATP binding site in the tertiary structure of RET kinase (e.g., amino acid positions 730-733, 738, 756, 758, 804. 805, 807, 811, 881, and 892 of a wildtype RET kinase, e.g., the exemplary wildtype RET kinase described herein), including but not limited to a gatekeeper residue (e.g., amino acid position 804 in a wildtype RET kinase), P-loop residues (e.g., amino acid positions 730-737 in a wildtype RET kinase), residues in or near the DFG motif (e.g., amino acid positions 888-898 in a wildtype RET kinase), and ATP cleft solvent front amino acid residues (e.g., amino acid positions 758, 811, and 892 of a wildtype RET kinase). Additional examples of these types of mutations include changes in residues that may affect enzyme activity and/or drug binding including but are not limited to residues in the activation loop (e.g., amino acid positions 891-916 of a wildtype RET kinase), residues near or interacting with the activation loop, residues contributing to active or inactive enzyme conformations, changes including mutations, deletions, and insertions in the loop proceeding the C-helix and in the C-helix (e.g., amino acid positions 768-788 in a wildtype RET protein). In some embodiments, the wildtype RET protein is the exemplary wildtype RET kinase described herein. Specific residues or residue regions that may be changed (and are RET inhibitor resistance mutations) include but are not limited to those listed in Table 3, with numbering based on the human wildtype RET protein sequence (e.g., SEQ ID NO: 1). As can be appreciated by those skilled in the art, an amino acid position in a reference protein sequence that corresponds to a specific amino acid position in SEQ ID NO: 1 can be determined by aligning the reference protein sequence with SEQ ID NO: 1 (e.g., using a software program, such as ClustalW2). Additional examples of RET inhibitor resistance mutation positions are shown in Table 4. Changes to these residues may include single or multiple amino acid changes, insertions within or flanking the sequences, and deletions within or flanking the sequences. See also J. Kooistra, G. K. Kanev, O. P. J. Van Linden, R. Leurs, I. J. P. De Esch, and C. De Graaf, “KLIFS: A structural kinase-ligand interaction database,” Nucleic Acids Res., vol. 44, no. D1, pp. D365-D371, 2016, which is incorporated by reference in its entirety herein.

Exemplary Sequence of Mature Human RET Protein (SEQ. ID NO: 1) MAKATSGAAG LRLLLLLLLP LLGKVALGLY FSRDAYWEKL YVDQAAGTPL LYVHALRDAP EEVPSFRLGQ HLYGTYRTRL HENNWICIQE DTGLLYLNRS LDHSSWEKLS VRNRGFPLLT VYLKVFLSPT SLREGECQWP GCARVYFSFF NTSFPACSSL KPRELCFPET RPSFRIRENR PPGTFHQFRL LPVQFLCPNI SVAYRLLEGE GLPFRCAPDS LEVSTRWALD REQREKYELV AVCTVHAGAR EEVVMVPFPV TVYDEDDSAP TFPAGVDTAS AVVEFKRKED TVVATLRVFD ADVVPASGEL VRRYTSTLLP GDTWAQQTFR VEHWPNETSV QANGSFVRAT VHDYRLVLNR NLSISENRTM QLAVLVNDSD FQGPGAGVLL LHFNVSVLPV SLHLPSTYSL SVSRRARRFA QIGKVCVENC QAFSGINVQY KLHSSGANCS TLGVVTSAED TSGILFVNDT KALRRPKCAE LHYMVVATDQ QTSRQAQAQL LVTVEGSYVA EEAGCPLSCA VSKRRLECEE CGOLGSPTGR CEWRQGDGKG ITRNFSTCSP STKTCPDGHC DVVETQDINI CPQDCLRGSI VGGHEPGEPR GIKAGYGTCN CFPEEEKCFC EPEDIQDPLC DELCRTVIAA AVLFSFIVSV LLSAFCIHCY HKFAHKPPIS SAEMTFRRPA QAFPVSYSSS GARRPSLDSM ENQVSVDAFK ILEDPKWEFP RKNLVLGKTL GEGEFGKVVK ATAFHLKGRA GYTTVAVKML KENASPSELR DLLSEFNVLK QVNHPHVIKL YGACSQDGPL LLIVEYAKYG SLRGFLRESR KVGPGYLGSG GSRNSSSLDH PDERALTMGD LISFAWQISQ GMQYLAEMKL VHRDLAARNI LVAEGRKMKI SDFGLSRDVY EEDSYVKRSQ GRIPVKWMAI ESLFDHIYTT QSDVWSFGVL LWEIVTLOGN PYPGIPPERL FNLLKTGHRM ERPDNCSEEM YRLMLQCWKQ EPDKRPVFAD ISKDLEKMMV KRRDYLDLAA STPSDSLIYD DGLSEEETPL VDCNNAPLPR ALPSTWIENK LYGMSDPNWP GESPVPLTRA DGTNTGFPRY PNDSVYANWM LSPSAAKLMD TFDS

In some embodiments, compounds of Formula I and pharmaceutically acceptable salts and solvates are useful in treating patients that develop cancers with RET inhibitor resistance mutations (e.g., that result in an increased resistance to a first RET inhibitor, e.g., a substitution at amino acid position 804, e.g., V804M, V804L, or V804E, and/or one or more RET inhibitor resistance mutations listed in Tables 3 and 4) by either dosing in combination or as a subsequent or additional (e.g., follow-up) therapy to existing drug treatments (e.g., other RET kinase inhibitors; e.g., first and/or second RET kinase inhibitors). Exemplary first and second RET kinase inhibitors are described herein. In some embodiments, a first or second RET kinase inhibitor can be selected from the group consisting of cabozantinib, vandetanib, alectinib, apatinib, sitravatinib, sorafenib, lenvatinib, ponatinib, dovitinib, sunitinib, foretinib, LOXO-292, BLU667, and BLU6864.

In some embodiments, compounds of Formula I or pharmaceutically acceptable salts and solvates thereof are useful for treating a cancer that has been identified as having one or more RET inhibitor resistance mutations (that result in an increased resistance to a first or second RET inhibitor, e.g., a substitution at amino acid position 804, e.g., V804M, V804L, or V804E). Non-limiting examples of RET inhibitor resistance mutations are listed in Tables 3 and 4.

TABLE 3 RET Inhibitor Resistance Mutations Exemplary RET Resistance Mutations Amino acid position 732 (e.g., E732K)⁷ Amino acid position 788 (e.g., I788N)⁸ Amino acid position 790 (e.g., L790F)⁹ Amino acid position 804 (e.g., V804M^(1, 2), V804L^(1, 2), V804E⁶) Amino acid position 804/805 (e.g., V804M/E805K)³ Amino acid position 806 (e.g., Y806C^(4,6), Y806E⁴, Y806S⁶, Y806H⁶, Y806N⁶) Amino acid position 810 (e.g., G810A⁵, G810R⁶, G810S⁶) Amino acid position 865 (e.g., L865V⁶) Amino acid position 870 (e.g., L870F⁶) ¹Yoon et al., J. Med. Chem. 59(1): 358-73, 2016. ² U.S. Pat. No. 8,629,135. ³Cranston, et al., Cancer Res. 66(20): 10179-87, 2006. ⁴Carlomagno, et al., Endocr. Rel. Cancer 16(1): 233-41, 2009. ⁵Huang et al., Mol. Cancer Ther., 2016 Aug. 5. pii: molcanther.0258.2016. [Epub ahead of print]. ⁶PCT Patent Application Publication No. WO 2016/127074. ⁷Mamedova et al., Summer Undergraduate Research Programs (SURP) Student Abstracts, University of Oklahoma Health Sciences Center, 2016. ⁸Plenker et al., Sci. Transl. Med., 9(394), doi: 10.1126/scitranslmed.aah6144, 2017. ⁹Kraft et al, Cancer Research, 2017, Vol. 77, No. 13, Supp. Supplement 1. Abstract Number: 4882; American Association for Cancer Research Annual Meeting 2017. Washington, DC, United States. 1 Apr. 2017-5 Apr. 2017.

TABLE 4 Additional Exemplary Amino Acid Positions of RET Inhibitor Resistance Mutations RET Amino Acid Exemplary and Position Mutation Mechanistic Resistance Rationale L730 P Steric hindrance and/or active conformational effect G731 V Steric hindrance and/or active conformational effect E732 K Steric hindrance and/or active conformational effect G733 V Steric hindrance and/or active conformational effect E734 K Steric hindrance and/or active conformational effect L760 M Active conformational effect K761 E Active conformational effect E762 K Active conformational effect N763 D Active conformational effect A764 V Active conformational effect S765 N Active conformational effect P766 A Active conformational effect S767 C Active conformational effect E768 K Active conformational effect L779 M Steric hindrance and/or active conformational effect I788 M Steric hindrance and/or active conformational effect M868 R Steric hindrance and/or active conformational effect K869 E Steric hindrance and/or active conformational effect L870 Q Steric hindrance and/or active conformational effect V871 M Steric hindrance and/or active conformational effect H872 R Steric hindrance and/or active conformational effect R873 P Steric hindrance and/or active conformational effect D874 Y Steric hindrance and/or active conformational effect L881 R Steric hindrance and/or active conformational effect L895 M Active conformational effect S896 N Active conformational effect R897 C Active conformational effect D898 Y Active conformational effect V899 G Active conformational effect Y900 D Active conformational effect E901 K Active conformational effect E902 K Active conformational effect D903 Y Active conformational effect S904 C Active conformational effect Y905 D Active conformational effect V906 M Active conformational effect K907 E Active conformational effect R908 P Active conformational effect S909 C Active conformational effect Q910 R Active conformational effect G911 C Active conformational effect R912 P Active conformational effect

The oncogenic role of RET was firstly described in papillary thyroid carcinoma (PTC) (Grieco et al., Cell, 1990, 60, 557-63), which arises from follicular thyroid cells and is the most common thyroid malignancy. Approximately 20-30% of PTC harbor somatic chromosomal rearrangements (translocations or inversions) linking the promoter and the 5′ portions of constitutively expressed, unrelated genes to the RET tyrosine kinase domain (Greco et al., Q. J. Nucl. Med. Mol. Imaging, 2009, 53, 440-54), therefore driving its ectopic expression in thyroid cells. Fusion proteins generated by such rearrangements are termed “RET/PTC” proteins. For example, RET/PTC 1 is a fusion between CCDD6 and RET that is commonly found in papillary thyroid carcinomas. Similarly, both RET/PTC3 and RET/PTC4 are fusions of ELE1 and RET that are commonly found in papillary thyroid carcinomas, although the fusion events resulting RET/PTC3 and RET/PTC4 lead to different proteins with different molecular weights (see e.g., Fugazzola et al., Oncogene, 13(5):1093-7, 1996). Some RET fusions associated with PTC are not referred to as “RET/PTC”, but instead are referred to as the fusion protein inself. For example, fusion between RET and both ELKS and PCM1 are found in PTCs, but the fusion proteins are referred to as ELKS-RET and PCM1-RET (see e.g., Romei and Elisei, Front. Endocrinol. (Lausanne), 3:54, doi: 10.3389/fendo.2012.00054, 2012). The role of RET-PTC rearrangements in the pathogenesis of PTC has been confirmed in transgenic mice (Santoro et al., Oncogene, 1996, 12, 1821-6). To date, a variety of fusion partners have been identified, from PTC and other cancer types, all providing a protein/protein interaction domain that induces ligand-independent RET dimerization and constitutive kinase activity (see, e.g., Table 1). Recently, a 10.6 Mb pericentric inversion in chromosome 10, where RET gene maps, has been identified in about 2% of lung adenocarcinoma patients, generating different variants of the chimeric gene KIF5B-RET (Ju et al., Genome Res., 2012, 22, 436-45; Kohno et al., 2012, Nature Med., 18, 375-7; Takeuchi et al., Nature Med., 2012, 18, 378-81; Lipson et al., 2012, Nature Med., 18, 382-4). The fusion transcripts are highly expressed and all the resulting chimeric proteins contain the N-terminal portion of the coiled-coil region of KIF5B, which mediates homodimerization, and the entire RET kinase domain. None of RET positive patients harbor other known oncogenic alterations (such as EGFR or K-Ras mutation, ALK translocation), supporting the possibility that KIF5B-RET fusion could be a driver mutation of lung adenocarcinoma. The oncogenic potential of KIF5B-RET has been confirmed by transfecting the fusion gene into cultured cell lines: similarly to what has been observed with RET-PTC fusion proteins, KIF5B-RET is constitutively phosphorylated and induces NIH-3T3 transformation and IL-3 independent growth of BA-F3 cells. However, other RET fusion proteins have been identified in lung adenocarcinoma patients, such as the CCDC6-RET fusion protein, which has been found to play a key role in the proliferation of the human lung adenocarcinoma cell line LC-2/ad (Journal of Thoracic Oncology, 2012, 7(12):1872-1876). RET inhibitors have been shown to be useful in treating lung cancers involving RET rearrangements (Drilon, A. E. et al. J Clin Oncol 33, 2015 (suppl; abstr 8007)). RET fusion proteins have also been identified in patients having colorectal cancer (Song Eun-Kee, et al. International Journal of Cancer, 2015, 136: 1967-1975).

Besides rearrangements of the RET sequence, gain of function point mutations of RET proto-oncogene are also driving oncogenic events, as shown in medullary thyroid carcinoma (MTC), which arises from parafollicular calcitonin-producing cells (de Groot, et al., Endocrine Rev., 2006, 27, 535-60; Wells and Santoro, Clin. Cancer Res., 2009, 15, 7119-7122). Around 25% of MTC are associated with multiple endocrine neoplasia type 2 (MEN2), a group of inherited cancer syndromes affecting neuroendocrine organs caused by germline activating point mutations of RET. In MEN2 subtypes (MEN2A, MEN2B and Familial MTC/FMTC) RET gene mutations have a strong phenotype-genotype correlation defining different MTC aggressiveness and clinical manifestations of the disease. In MEN2A syndrome mutations involve one of the six cysteine residues (mainly C634) located in the cysteine-rich extracellular region, leading to ligand-independent homodimerization and constitutive RET activation. Patients develop MTC at a young age (onset at 5-25 years) and may also develop pheochromocytoma (50%) and hyperparathyroidism. MEN2B is mainly caused by M918T mutation, which is located in the kinase domain. This mutation constitutively activates RET in its monomeric state and alters substrate recognition by the kinase. MEN2B syndrome is characterized by an early onset (<1 year) and very aggressive form of MTC, pheochromocytoma (50% of patients) and ganglioneuromas. In FMTC the only disease manifestation is MTC, usually occurring at an adult age. Many different mutations have been detected, spanning the entire RET gene. The remaining 75% of MTC cases are sporadic and about 50% of them harbor RET somatic mutations: the most frequent mutation is M918T that, as in MEN2B, is associated with the most aggressive phenotype. Somatic point mutations of RET have also been described in other tumors such as colorectal cancer (Wood et al., Science, 2007, 318, 1108-13) and small cell lung carcinoma (Jpn. J. Cancer Res., 1995, 86, 1127-30).

RET signaling components have been found to be expressed in primary breast tumors and to functionally interact with estrogen receptor-cc pathway in breast tumor cell lines (Boulay et al., Cancer Res. 2008, 68, 3743-51; Plaza-Menacho et al., Oncogene, 2010, 29, 4648-57), while RET expression and activation by GDNF family ligands could play an important role in perineural invasion by different types of cancer cells (Ito et al., Surgery, 2005, 138, 788-94; Gil et al., J. Natl. Cancer Inst., 2010, 102, 107-18; Iwahashi et al., Cancer, 2002, 94, 167-74).

RET is also expressed in 30-70% of invasive breast cancers, with expression being relatively more frequent in estrogen receptor-positive tumors (Plaza-Menacho, I., et al., Oncogene, 2010, 29, 4648-4657; Esseghir, S., et al., Cancer Res., 2007, 67, 11732-11741; Morandi, A., et al., Cancer Res., 2013, 73, 3783-3795; Gattelli, A., EMBO Mol. Med., 2013, 5, 1335-1350).

The identification of RET rearrangements has been reported in a subset of (patient-derived xenograft) PDX established from colorectal cancer. Although the frequency of such events in colorectal cancer patients remains to be defined, these data suggest a role of RET as a target in this indication (Gozgit et al., AACR Annual Meeting 2014). Studies have shown that the RET promoter is frequently methylated in colorectal cancers, and heterozygous missense mutations, which are predicted to reduce RET expression, are identified in 5-10% of cases, which suggests that RET might have some features of a tumor suppressor in sporadic colon cancers (Luo, Y., et al., Oncogene, 2013, 32, 2037-2047; Sjoblom, T., et al., Science, 2006, 268-274; Cancer Genome Atlas Network, Nature, 2012, 487, 330-337).

An increasing number of tumor types are now being shown to express substantial levels of wild-type RET kinase that could have implications for tumor progression and spread. RET is expressed in 50-65% of pancreatic ductal carcinomas, and expression is more frequent in metastatic and higher grade tumors (Ito, Y, et al., Surgery, 2005, 138, 788-794; Zeng, Q., et al., J. Int. Med. Res. 2008, 36, 656-664).

In neoplasms of hematopoietic lineages, RET is expressed in acute myeloid leukemia (AML) with monocytic differentiation, as well as in CMML (Gattei, V. et al., Blood, 1997, 89, 2925-2937; Gattei, V., et al., Ann. Hematol, 1998, 77, 207-210; Camos, M., Cancer Res. 2006, 66, 6947-6954). Recent studies have identified rare chromosomal rearrangements that involve RET in patients with chronic myelomonocytic leukemia (CMML). CMML is frequently associated with rearrangements of several tyrosine kinases, which result in the expression of chimeric cytosolic oncoproteins that lead to activation of RAS pathways (Kohlmann, A., et al., J. Clin. Oncol. 2010, 28, 2858-2865). In the case of RET, gene fusions that link RET with BCR (BCR-RET) or with fibroblast growth factor receptor 1 oncogene partner (FGFR1OP-RET) were transforming in early hematopoietic progenitor cells and could shift maturation of these cells towards monocytic paths, probably through the initiation of RET-mediated RAS signaling (Ballerini, P., et al., Leukemia, 2012, 26, 2384-2389).

RET expression has also been shown to occur in several other tumor types, including prostate cancer, small-cell lung carcinoma, melanoma, renal cell carcinoma, and head and neck tumors (Narita, N., et al., Oncogene, 2009, 28, 3058-3068; Mulligan, L. M., et al., Genes Chromosomes Cancer, 1998, 21, 326-332; Flavin, R., et al., Urol. Oncol., 2012, 30, 900-905; Dawson, D. M., J Natl Cancer Inst, 1998, 90, 519-523).

In neuroblastoma, RET expression and activation by GFLs has roles in tumor cell differentiation, potentially collaborating with other neurotrophic factor receptors to down regulate N-Myc, the expression of which is a marker of poor prognosis (Hofstra, R. M., W., et al., Hum. Genet. 1996, 97, 362-364; Petersen, S. and Bogenmann, E., Oncogene, 2004, 23, 213-225; Brodeur, G. M., Nature Ref. Cancer, 2003, 3, 203-216).

Multitargeted inhibitors which cross react with RET are known (Borrello, M. G., et al., Expert Opin. Ther. Targets, 2013, 17(4), 403-419; International Patent Application Nos. WO 2014/141187, WO 2014/184069, and WO 2015/079251). Such multitargeted inhibitors (or multikinase inhibitors or MKIs) can also be associated with development of RET inhibitor resistance mutations. See, for example, Q. Huang et al., “Preclinical Modeling of KIF5B-RET Fusion Lung Adenocarcinoma.,” Mol. Cancer Ther., no. 18, pp. 2521-2529, 2016; Yasuyuki Kaneta et al., Abstract B173: Preclinical characterization and antitumor efficacy of DS-5010, a highly potent and selective RET inhibitor, Mol Cancer Ther Jan. 1 2018 (17) (1 Supplement) B173; DOI:10.1158/1535-7163.TARG-17-B173, both of which are incorporated by reference in their entirety herein.

Accordingly, provided herein are methods for treating a patient diagnosed with (or identified as having) a cancer that include administering to the patient a therapeutically effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof. Also provided herein are methods for treating a patient identified or diagnosed as having a RET-associated cancer that include administering to the patient a therapeutically effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof or a pharmaceutical composition thereof. In some embodiments, the patient that has been identified or diagnosed as having a RET-associated cancer through the use of a regulatory agency-approved, e.g., FDA-approved test or assay for identifying dysregulation of a RET gene, a RET kinase, or expression or activity or level of any of the same, in a patient or a biopsy sample from the patient or by performing any of the non-limiting examples of assays described herein. In some embodiments, the test or assay is provided as a kit. In some embodiments, the cancer is a RET-associated cancer. For example, the RET-associated cancer can be a cancer that includes one or more RET inhibitor resistance mutations.

Also provided are methods for treating cancer in a patient in need thereof, the method comprising: (a) detecting a RET-associated cancer in the patient; and (b) administering to the patient a therapeutically effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof or a pharmaceutical composition thereof. Some embodiments of these methods further include administering to the subject another anticancer agent (e.g., a second RET inhibitor, a second compound of Formula I or a pharmaceutically acceptable salt or solvate thereof, or an immunotherapy). In some embodiments, the subject was previously treated with a first RET inhibitor or previously treated with another anticancer treatment, e.g., resection of the tumor or radiation therapy. In some embodiments, the patient is determined to have a RET-associated cancer through the use of a regulatory agency-approved, e.g., FDA-approved test or assay for identifying dysregulation of a RET gene, a RET kinase, or expression or activity or level of any of the same, in a patient or a biopsy sample from the patient or by performing any of the non-limiting examples of assays described herein. In some embodiments, the test or assay is provided as a kit. In some embodiments, the cancer is a RET-associated cancer. For example, the RET-associated cancer can be a cancer that includes one or more RET inhibitor resistance mutations.

Also provided are methods of treating a patient that include performing an assay on a sample obtained from the patient to determine whether the patient has a dysregulation of a RET gene, a RET kinase, or expression or activity or level of any of the same, and administering (e.g., specifically or selectively administering) a therapeutically effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof or a pharmaceutical composition thereof to the patient determined to have a dysregulation of a RET gene, a RET kinase, or expression or activity or level of any of the same. Some embodiments of these methods further include administering to the subject another anticancer agent (e.g., a second RET inhibitor, a second compound of Formula I or a pharmaceutically acceptable salt or solvate thereof, or immunotherapy). In some embodiments of these methods, the subject was previously treated with a first RET inhibitor or previously treated with another anticancer treatment, e.g., resection of a tumor or radiation therapy. In some embodiments, the patient is a patient suspected of having a RET-associated cancer, a patient presenting with one or more symptoms of a RET-associated cancer, or a patient having an elevated risk of developing a RET-associated cancer. In some embodiments, the assay utilizes next generation sequencing, pyrosequencing, immunohistochemistry, or break apart FISH analysis. In some embodiments, the assay is a regulatory agency-approved assay, e.g., FDA-approved kit. In some embodiments, the assay is a liquid biopsy. Additional, non-limiting assays that may be used in these methods are described herein. Additional assays are also known in the art. In some embodiments, the dysregulation of a RET gene, a RET kinase, or expression or activity or level of any of the same includes one or more RET inhibitor resistance mutations.

Also provided is a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof or a pharmaceutical composition thereof for use in treating a RET-associated cancer in a patient identified or diagnosed as having a RET-associated cancer through a step of performing an assay (e.g., an in vitro assay) on a sample obtained from the patient to determine whether the patient has a dysregulation of a RET gene, a RET kinase, or expression or activity or level of any of the same, where the presence of a dysregulation of a RET gene, a RET kinase, or expression or activity or level of any of the same, identifies that the patient has a RET-associated cancer. Also provided is the use of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof for the manufacture of a medicament for treating a RET-associated cancer in a patient identified or diagnosed as having a RET-associated cancer through a step of performing an assay on a sample obtained from the patient to determine whether the patient has a dysregulation of a RET gene, a RET kinase, or expression or activity or level of any of the same where the presence of dysregulation of a RET gene, a RET kinase, or expression or activity or level of any of the same, identifies that the patient has a RET-associated cancer. Some embodiments of any of the methods or uses described herein further include recording in the patient's clinical record (e.g., a computer readable medium) that the patient is determined to have a dysregulation of a RET gene, a RET kinase, or expression or activity or level of any of the same, through the performance of the assay, should be administered a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof or a pharmaceutical composition thereof. In some embodiments, the assay utilizes next generation sequencing, pyrosequencing, immunohistochemistry, or break apart FISH analysis. In some embodiments, the assay is a regulatory agency-approved assay, e.g., FDA-approved kit. In some embodiments, the assay is a liquid biopsy. In some embodiments, the dysregulation of a RET gene, a RET kinase, or expression or activity or level of any of the same includes one or more RET inhibitor resistance mutations.

Also provided is a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof, for use in the treatment of a cancer in a patient in need thereof or a patient identified or diagnosed as having a RET-associated cancer. Also provided is the use of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof for the manufacture of a medicament for treating a cancer in a patient identified or diagnosed as having a RET-associated cancer. In some embodiments, the cancer is a RET-associated cancer, for example, a RET-associated cancer having one or more RET inhibitor resistance mutations. In some embodiments, a patient is identified or diagnosed as having a RET-associated cancer through the use of a regulatory agency-approved, e.g., FDA-approved, kit for identifying dysregulation of a RET gene, a RET kinase, or expression or activity or level of any of the same, in a patient or a biopsy sample from the sample. As provided herein, a RET-associated cancer includes those described herein and known in the art.

In some embodiments of any of the methods or uses described herein, the patient has been identified or diagnosed as having a cancer with a dysregulation of a RET gene, a RET kinase, or expression or activity or level of any of the same. In some embodiments of any of the methods or uses described herein, the patient has a tumor that is positive for a dysregulation of a RET gene, a RET kinase, or expression or activity or level of any of the same. In some embodiments of any of the methods or uses described herein, the patient can be a patient with a tumor(s) that is positive for a dysregulation of a RET gene, a RET kinase, or expression or activity or level of any of the same. In some embodiments of any of the methods or uses described herein, the patient can be a patient whose tumors have a dysregulation of a RET gene, a RET kinase, or expression or activity or level of any of the same. In some embodiments of any of the methods or uses described herein, the patient is suspected of having a RET-associated cancer (e.g., a cancer having one or more RET inhibitor resistance mutations). In some embodiments, provided herein are methods for treating a RET-associated cancer in a patient in need of such treatment, the method comprising a) detecting a dysregulation of a RET gene, a RET kinase, or the expression or activity or level of any of the same in a sample from the patient; and b) administering a therapeutically effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the dysregulation of a RET gene, a RET kinase, or the expression or activity or level of any of the same includes one or more fusion proteins. Non-limiting examples of RET gene fusion proteins are described in Table 1. In some embodiments, the fusion protein is KIF5B-RET. In some embodiments, the dysregulation of a RET gene, a RET kinase, or the expression or activity or level of any of the same includes one or more RET kinase protein point mutations/insertions/deletions. Non-limiting examples of RET kinase protein point mutations/insertions/deletions are described in Tables 2 and 2a. In some embodiments, the RET kinase protein point mutations/insertions/deletions are selected from the group consisting of M918T, M918V, C634W, V804L, and V804M. In some embodiments, the dysregulation of a RET gene, a RET kinase, or the expression or activity or level of any of the same includes one or more RET inhibitor resistance mutations. Non-limiting examples of RET inhibitor resistance mutations are described in Tables 3 and 4. In some embodiments, the RET inhibitor resistance mutation is V804M. In some embodiments, the cancer with a dysregulation of a RET gene, a RET kinase, or expression or activity or level of any of the same is determined using a regulatory agency-approved, e.g., FDA-approved, assay or kit. In some embodiments, the tumor that is positive for a dysregulation of a RET gene, a RET kinase, or expression or activity or level of any of the same is a tumor positive for one or more RET inhibitor resistance mutations. In some embodiments, the tumor with a dysregulation of a RET gene, a RET kinase, or expression or activity or level of any of the same is determined using a regulatory agency-approved, e.g., FDA-approved, assay or kit.

In some embodiments of any of the methods or uses described herein, the patient has a clinical record indicating that the patient has a tumor that has a dysregulation of a RET gene, a RET kinase, or expression or activity or level of any of the same (e.g., a tumor having one or more RET inhibitor resistance mutations). In some embodiments, the clinical record indicates that the patient should be treated with one or more of the compounds of Formula I or a pharmaceutically acceptable salts or solvates thereof or compositions provided herein. In some embodiments, the cancer with a dysregulation of a RET gene, a RET kinase, or expression or activity or level of any of the same is a cancer having one or more RET inhibitor resistance mutations. In some embodiments, the cancer with a dysregulation of a RET gene, a RET kinase, or expression or activity or level of any of the same is determined using a regulatory agency-approved, e.g., FDA-approved, assay or kit. In some embodiments, the tumor that is positive for a dysregulation of a RET gene, a RET kinase, or expression or activity or level of any of the same is a tumor positive for one or more RET inhibitor resistance mutations. In some embodiments, the tumor with a dysregulation of a RET gene, a RET kinase, or expression or activity or level of any of the same is determined using a regulatory agency-approved, e.g., FDA-approved, assay or kit.

Also provided are methods of treating a patient that include administering a therapeutically effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof to a patient having a clinical record that indicates that the patient has a dysregulation of a RET gene, a RET kinase, or expression or activity or level of any of the same. Also provided is the use of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof for the manufacture of a medicament for treating a RET-associated cancer in a patient having a clinical record that indicates that the patient has a dysregulation of a RET gene, a RET kinase, or expression or activity or level of any of the same. Some embodiments of these methods and uses can further include: a step of performing an assay (e.g., an in vitro assay) on a sample obtained from the patient to determine whether the patient has a dysregulation of a RET gene, a RET kinase, or expression or activity or level of any of the same, and recording the information in a patient's clinical file (e.g., a computer readable medium) that the patient has been identified to have a dysregulation of a RET gene, a RET kinase, or expression or activity or level of any of the same. In some embodiments, the assay is an in vitro assay. For example, an assay that utilizes next generation sequencing, immunohistochemistry, or break apart FISH analysis. In some embodiments, the assay is a regulatory agency-approved, e.g., FDA-approved, kit. In some embodiments, the assay is a liquid biopsy. In some embodiments, the dysregulation of a RET gene, RET kinase, or expression or activity or level of any of the same includes one or more RET inhibitor resistance mutations.

Also provided herein is a method of treating a subject. In some embodiments, the method includes performing an assay on a sample obtained from the subject to determine whether the subject has a dysregulation of a RET gene, a RET protein, or expression or level of any of the same. In some such embodiments, the method also includes administering to a subject determined to have a dysregulation of a RET gene, a RET protein, or expression or activity, or level of any of the same a therapeutically effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the method includes determining that a subject has a dysregulation of a RET gene, a RET protein, or expression or level of any of the same via an assay performed on a sample obtained from the subject. In such embodiments, the method also includes administering to a subject a therapeutically effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the dysregulation in a RET gene, a RET kinase protein, or expression or activity of the same is a gene or chromosome translocation that results in the expression of a RET fusion protein (e.g., any of the RET fusion proteins described herein). In some embodiments, the RET fusion can be selected from a KIF5B-RET fusion and a CCDC6-RET fusion. In some embodiments, the dysregulation in a RET gene, a RET kinase protein, or expression or activity or level of any of the same is one or more point mutation in the RET gene (e.g., any of the one or more of the RET point mutations described herein). The one or more point mutations in a RET gene can result, e.g., in the translation of a RET protein having one or more of the following amino acid substitutions: M918T, M918V, C634W, V804L, and V804M. In some embodiments, the dysregulation in a RET gene, a RET kinase protein, or expression or activity or level of any of the same is one or more RET inhibitor resistance mutations (e.g., any combination of the one or more RET inhibitor resistance mutations described herein). Some embodiments of these methods further include administering to the subject another anticancer agent (e.g., a second RET inhibitor a second compound of Formula I or a pharmaceutically acceptable salt or solvate thereof, or immunotherapy).

In some embodiments, the compounds provided herein exhibit brain and/or central nervous system (CNS) penetrance. Such compounds are capable of crossing the blood brain barrier and inhibiting a RET kinase in the brain and/or other CNS structures. In some embodiments, the compounds provided herein are capable of crossing the blood brain barrier in a therapeutically effective amount. For example, treatment of a patient with cancer (e.g., a RET-associated cancer such as a RET-associated brain or CNS cancer) can include administration (e.g., oral administration) of the compound to the patient. In some such embodiments, the compounds provided herein are useful for treating a primary brain tumor or metastatic brain tumor. For example, the compounds can be used in the treatment of one or more of gliomas such as glioblastoma (also known as glioblastoma multiforme), astrocytomas, oligodendrogliomas, ependymomas, and mixed gliomas, meningiomas, medulloblastomas, gangliogliomas, schwannomas (neurilemmomas), and craniopharyngiomas (see, for example, the tumors listed in Louis, D. N. et al. Acta Neuropathol 131(6), 803-820 (June 2016)). In some embodiments, the brain tumor is a primary brain tumor. In some embodiments, the patient has previously been treated with another anticancer agent, e.g., another RET inhibitor (e.g., a compound that is not a compound of General Formula I) or a multi-kinase inhibitor. In some embodiments, the brain tumor is a metastatic brain tumor. In some embodiments, the patient has previously been treated with another anticancer agent, e.g., another RET inhibitor (e.g., a compound that is not a compound of General Formula I) or a multi-kinase inhibitor.

Also provided are methods (e.g., in vitro methods) of selecting a treatment for a patient identified or diagnosed as having a RET-associated cancer. Some embodiments can further include administering the selected treatment to the patient identified or diagnosed as having a RET-associated cancer. For example, the selected treatment can include administration of a therapeutically effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof. Some embodiments can further include a step of performing an assay on a sample obtained from the patient to determine whether the patient has a dysregulation of a RET gene, a RET kinase, or expression or activity or level of any of the same, and identifying and diagnosing a patient determined to have a dysregulation of a RET gene, a RET kinase, or expression or activity or level of any of the same, as having a RET-associated cancer. In some embodiments, the cancer is a RET-associated cancer having one or more RET inhibitor resistance mutations. In some embodiments, the patient has been identified or diagnosed as having a RET-associated cancer through the use of a regulatory agency-approved, e.g., FDA-approved, kit for identifying dysregulation of a RET gene, a RET kinase, or expression or activity or level of any of the same, in a patient or a biopsy sample from the patient. In some embodiments, the RET-associated cancers is a cancer described herein or known in the art. In some embodiments, the assay is an in vitro assay. For example, an assay that utilizes the next generation sequencing, immunohistochemistry, or break apart FISH analysis. In some embodiments, the assay is a regulatory agency-approved, e.g., FDA-approved, kit. In some embodiments, the assay is a liquid biopsy.

Also provided herein are methods of selecting a treatment for a patient, wherein the methods include a step of performing an assay on a sample obtained from the patient to determine whether the patient has a dysregulation of a RET gene, a RET kinase, or expression or activity or level of any of the same (e.g., one or more RET inhibitor resistance mutations), and identifying or diagnosing a patient determined to have a dysregulation of a RET gene, a RET kinase, or expression or activity or level of any of the same, as having a RET-associated cancer. Some embodiments further include administering the selected treatment to the patient identified or diagnosed as having a RET-associated cancer. For example, the selected treatment can include administration of a therapeutically effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof to the patient identified or diagnosed as having a RET-associated cancer. In some embodiments, the assay is an in vitro assay. For example, an assay that utilizes the next generation sequencing, immunohistochemistry, or break apart FISH analysis. In some embodiments, the assay is a regulatory agency-approved, e.g., FDA-approved, kit. In some embodiments, the assay is a liquid biopsy.

Also provided are methods of selecting a patient for treatment, wherein the methods include selecting, identifying, or diagnosing a patient having a RET-associated cancer, and selecting the patient for treatment including administration of a therapeutically-effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, identifying or diagnosing a patient as having a RET-associated cancer can include a step of performing an assay on a sample obtained from the patient to determine whether the patient has a dysregulation of a RET gene, a RET kinase, or expression or activity or level of any of the same, and identifying or diagnosing a patient determined to have a dysregulation of a RET gene, a RET kinase, or expression or activity or level of any of the same, as having a RET-associated cancer. In some embodiments, the method of selecting a patient for treatment can be used as a part of a clinical study that includes administration of various treatments of a RET-associated cancer. In some embodiments, a RET-associated cancer is a cancer having one or more RET inhibitor resistance mutations. In some embodiments, the assay is an in vitro assay. For example, an assay that utilizes the next generation sequencing, immunohistochemistry, or break apart FISH analysis. In some embodiments, the assay is a regulatory agency-approved, e.g., FDA-approved, kit. In some embodiments, the assay is a liquid biopsy. In some embodiments, the dysregulation of the RET gene, the RET kinase, or expression or activity or level of any of the same includes one or more RET inhibitor resistance mutations.

In some embodiments of any of the methods or uses described herein, an assay used to determine whether the patient has a dysregulation of a RET gene, or a RET kinase, or expression or activity or level of any of the same, using a sample from a patient can include, for example, next generation sequencing, immunohistochemistry, fluorescence microscopy, break apart FISH analysis, Southern blotting, Western blotting, FACS analysis, Northern blotting, and PCR-based amplification (e.g., RT-PCR and quantitative real-time RT-PCR). As is well-known in the art, the assays are typically performed, e.g., with at least one labelled nucleic acid probe or at least one labelled antibody or antigen-binding fragment thereof. Assays can utilize other detection methods known in the art for detecting dysregulation of a RET gene, a RET kinase, or expression or activity or levels of any of the same (see, e.g., the references cited herein). In some embodiments, the dysregulation of the RET gene, the RET kinase, or expression or activity or level of any of the same includes one or more RET inhibitor resistance mutations. In some embodiments, the sample is a biological sample or a biopsy sample (e.g., a paraffin-embedded biopsy sample) from the patient. In some embodiments, the patient is a patient suspected of having a RET-associated cancer, a patient having one or more symptoms of a RET-associated cancer, and/or a patient that has an increased risk of developing a RET-associated cancer)

In some embodiments, dysregulation of a RET gene, a RET kinase, or the expression or activity or level of any of the same can be identified using a liquid biopsy (variously referred to as a fluid biopsy or fluid phase biopsy). See, e.g., Karachialiou et al., “Real-time liquid biopsies become a reality in cancer treatment”, Ann. Transl. Med., 3(3):36, 2016. Liquid biopsy methods can be used to detect total tumor burden and/or the dysregulation of a RET gene, a RET kinase, or the expression or activity or level of any of the same. Liquid biopsies can be performed on biological samples obtained relatively easily from a subject (e.g., via a simple blood draw) and are generally less invasive than traditional methods used to detect tumor burden and/or dysregulation of a RET gene, a RET kinase, or the expression or activity or level of any of the same. In some embodiments, liquid biopsies can be used to detect the presence of dysregulation of a RET gene, a RET kinase, or the expression or activity or level of any of the same at an earlier stage than traditional methods. In some embodiments, the biological sample to be used in a liquid biopsy can include, blood, plasma, urine, cerebrospinal fluid, saliva, sputum, broncho-alveolar lavage, bile, lymphatic fluid, cyst fluid, stool, ascites, and combinations thereof. In some embodiments, a liquid biopsy can be used to detect circulating tumor cells (CTCs). In some embodiments, a liquid biopsy can be used to detect cell-free DNA. In some embodiments, cell-free DNA detected using a liquid biopsy is circulating tumor DNA (ctDNA) that is derived from tumor cells. Analysis of ctDNA (e.g., using sensitive detection techniques such as, without limitation, next-generation sequencing (NGS), traditional PCR, digital PCR, or microarray analysis) can be used to identify dysregulation of a RET gene, a RET kinase, or the expression or activity or level of any of the same.

In some embodiments, ctDNA derived from a single gene can be detected using a liquid biopsy. In some embodiments, ctDNA derived from a plurality of genes (e.g., 2, 3, 4, 5, 6, 7, 8, 9, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 100 or more, or any number of genes in between these numbers) can be detected using a liquid biopsy. In some embodiments, ctDNA derived from a plurality of genes can be detected using any of a variety of commercially-available testing panels (e.g., commercially-available testing panels designed to detect dysregulation of a RET gene, a RET kinase, or the expression or activity or level of any of the same). Liquid biopsies can be used to detect dysregulation of a RET gene, a RET kinase, or the expression or activity or level of any of the same including, without limitation, point mutations or single nucleotide variants (SNVs), copy number variants (CNVs), genetic fusions (e.g., translocations or rearrangements), insertions, deletions, or any combination thereof. In some embodiments, a liquid biopsy can be used to detect a germline mutation. In some embodiments, a liquid biopsy can be used to detect a somatic mutation. In some embodiments, a liquid biopsy can be used to detect a primary genetic mutation (e.g., a primary mutation or a primary fusion that is associated with initial development of a disease, e.g., cancer). In some embodiments, a liquid biopsy can be used to detect a genetic mutation that develops after development of the primary genetic mutation (e.g., a resistance mutation that arises in response to a treatment administered to a subject). In some embodiments, a dysregulation of a RET gene, a RET kinase, or the expression or activity or level of any of the same identified using a liquid biopsy is also present in a cancer cell that is present in the subject (e.g., in a tumor). In some embodiments, any of the types of dysregulation of a RET gene, a RET kinase, or the expression or activity or level of any of the same described herein can be detected using a liquid biopsy. In some embodiments, a genetic mutation identified via a liquid biopsy can be used to identify the subject as a candidate for a particular treatment. For example, detection of dysregulation of a RET gene, a RET kinase, or the expression or activity or level of any of the same in the subject can indicate that the subject will be responsive to a treatment that includes administration of a compound of Formula I or a pharmaceutically acceptable salt thereof.

Liquid biopsies can be performed at multiple times during a course of diagnosis, a course of monitoring, and/or a course of treatment to determine one or more clinically relevant parameters including, without limitation, progression of the disease, efficacy of a treatment, or development of resistance mutations after administering a treatment to the subject. For example, a first liquid biopsy can be performed at a first time point and a second liquid biopsy can be performed at a second time point during a course of diagnosis, a course of monitoring, and/or a course of treatment. In some embodiments, the first time point can be a time point prior to diagnosing a subject with a disease (e.g., when the subject is healthy), and the second time point can be a time point after subject has developed the disease (e.g., the second time point can be used to diagnose the subject with the disease). In some embodiments, the first time point can be a time point prior to diagnosing a subject with a disease (e.g., when the subject is healthy), after which the subject is monitored, and the second time point can be a time point after monitoring the subject. In some embodiments, the first time point can be a time point after diagnosing a subject with a disease, after which a treatment is administered to the subject, and the second time point can be a time point after the treatment is administered; in such cases, the second time point can be used to assess the efficacy of the treatment (e.g., if the genetic mutation(s) detected at the first time point are reduced in abundance or are undetectable) or to determine the presence of a resistance mutation that has arisen as a result of the treatment. In some embodiments, a treatment to be administered to a subject can include a compound of Formula I or a pharmaceutically acceptable salt thereof.

In the field of medical oncology it is normal practice to use a combination of different forms of treatment to treat each patient with cancer. In medical oncology the other component(s) of such conjoint treatment or therapy in addition to compositions provided herein may be, for example, surgery, radiotherapy, and chemotherapeutic agents, such as other kinase inhibitors, signal transduction inhibitors and/or monoclonal antibodies. For example, a surgery may be open surgery or minimally invasive surgery. Compounds of Formula I therefore may also be useful as adjuvants to cancer treatment, that is, they can be used in combination with one or more additional therapies or therapeutic agents, for example a chemotherapeutic agent that works by the same or by a different mechanism of action.

In some embodiments of any the methods described herein, the compound of Formula I (or a pharmaceutically acceptable salt or solvate thereof) is administered in combination with a therapeutically effective amount of at least one additional therapeutic agent selected from one or more additional therapies or therapeutic (e.g., chemotherapeutic) agents.

Non-limiting examples of additional therapeutic agents include: other RET-targeted therapeutic agents (i.e. a first or second RET kinase inhibitor), receptor tyrosine kinase-targeted therapeutic agents, signal transduction pathway inhibitors, checkpoint inhibitors, modulators of the apoptosis pathway (e.g. obataclax); cytotoxic chemotherapeutics, angiogenesis-targeted therapies, immune-targeted agents, including immunotherapy, and radiotherapy. In some embodiments, the other RET-targeted therapeutic is a multikinase inhibitor exhibiting RET inhibition activity. In some embodiments, the other RET-targeted therapeutic inhibitor is selective for a RET kinase. Exemplary RET kinase inhibitors can exhibit inhibition activity (IC₅₀) against a RET kinase of less than about 1000 nM, less than about 500 nM, less than about 200 nM, less than about 100 nM, less than about 50 nM, less than about 25 nM, less than about 10 nM, or less than about 1 nM as measured in an assay as described herein. In some embodiments, a RET kinase inhibitors can exhibit inhibition activity (IC₅₀) against a RET kinase of less than about 25 nM, less than about 10 nM, less than about 5 nM, or less than about 1 nM as measured in an assay as provided herein.

Non-limiting examples of RET-targeted therapeutic agents (e.g., a first RET inhibitor or a second RET inhibitor) include alectinib (9-Ethyl-6,6-dimethyl-8-[4-(morpholin-4-yl)piperidin-1-yl]-11-oxo-6,11-dihydro-5H-benzo[b]carbazole-3-carbonitrile); amuvatinib (MP470, HPK56) (N-(1,3-benzodioxol-5-ylmethyl)-4-([1]benzofuro[3,2-d]pyrimidin-4-yl)piperazine-1-carbothioamide); apatinib (YN968D1) (N-[4-(1-cyanocyclopentyl) phenyl-2-(4-picolyl)amino-3-Nicotinamide methanesulphonate); cabozantinib (Cometriq XL-184) (N-(4-((6,7-Dimethoxyquinolin-4-yl)oxy)phenyl)-N′-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide); dovitinib (TK1258; GFKI-258; CHIR-258) ((3Z)-4-amino-5-fluoro-3-[5-(4-methylpiperazin-1-yl)-1,3-dihydrobenzimidazol-2-ylidene]quinolin-2-one); famitinib (5-[2-(diethylamino)ethyl]-2-[(Z)-(5-fluoro-2-oxo-1H-indol-3-ylidene)methyl]-3-methyl-6,7-dihydro-1H-pyrrolo[3,2-c]pyridin-4-one); fedratinib (SAR302503, TG101348) (N-(2-Methyl-2-propanyl)-3-{[5-methyl-2-({4-[2-(1-pyrrolidinyl)ethoxy]phenyl}amino)-4-pyrimidinyl]amino}benzenesulfonamide); foretinib (XL880, EXEL-2880, GSK1363089, GSK089) (N1′-[3-fluoro-4-[[6-methoxy-7-(3-morpholinopropoxy)-4-quinolyl]oxy]phenyl]-N1-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide); fostamantinib (R788) (2H-Pyrido[3,2-b]-1,4-oxazin-3 (4H)-one, 6-[[5-fluoro-2-[(3,4,5-trimethoxyphenyl)amino]-4-pyrimidinyl]amino]-2,2-dimethyl-4-[(phosphonooxy)methyl]-, sodium salt (1:2)); ilorasertib (ABT-348) (1-(4-(4-amino-7-(1-(2-hydroxyethyl)-1H-pyrazol-4-yl)thieno[3,2-c]pyridin-3-yl)phenyl)-3-(3-fluorophenyl)urea); lenvatinib (E7080, Lenvima) (4-[3-chloro-4-(cyclopropylaminocarbonyl)aminophenoxy]-7-methoxy-6-quinolinecarboxamide); motesanib (AMG 706) (N-(3,3-Dimethyl-2,3-dihydro-1H-indol-6-yl)-2-[(pyridin-4-ylmethyl)amino]pyridine-3-carboxamide); nintedanib (3-Z-[1-(4-(N-((4-methyl-piperazin-1-yl)-methylcarbonyl)-N-methyl-amino)-anilino)-1-phenyl-methylene]-6-methyoxycarbonyl-2-indolinone); ponatinib (AP24534) (3-(2-Imidazo[1,2-b]pyridazin-3-ylethynyl)-4-methyl-N-[4-[(4-methylpiperazin-1-yl)methyl]-3-(trifluoromethyl)phenyl]benzamide); PP242 (a TORKinib) (2-[4-Amino-1-(1-methylethyl)-1H-pyrazolo[3,4-d]pyrimidin-3-yl]-1H-indol-5-ol); quizartinib (1-(5-(tert-Butyl)isoxazol-3-yl)-3-(4-(7-(2-morpholinoethoxy)benzo[d]imidazo[2,1-b]thiazol-2-yl)phenyl)urea); regorfenib (BAY 73-4506, stivarga) (4-[4-({[4-Chloro-3-(trifluoromethyl)phenyl]carbamoyl}amino)-3-fluorophenoxy]-N-methylpyridine-2-carboxamide hydrate); RXDX-105 (CEP-32496, agerafenib) (1-(3-((6,7-dimethoxyquinazolin-4-yl)oxy)phenyl)-3-(5-(1,1,1-trifluoro-2-methylpropan-2-yl)isoxazol-3-yl)urea); semaxanib (SU5416) ((3Z)-3-[(3,5-dimethyl-1H-pyrrol-2-yl)methylidene]-1,3-dihydro-2H-indol-2-one); sitravatinib (MGCD516, MG516) (N-(3-Fluoro-4-{[2-(5-{[(2-methoxyethyl)amino]methyl}-2-pyridinyl)thieno[3,2-b]pyridin-7-yl]oxy}phenyl)-N?-(4-fluorophenyl)-1,1-cyclopropanedicarboxamide); sorafenib (BAY 43-9006) (4-[4-[[[[4-chloro-3-(trifluoromethyl)phenyl]amino]carbonyl]amino]phenoxy]-N-methyl-2-pyridinecarboxamide); vandetanib (N-(4-bromo-2-fluorophenyl)-6-methoxy-7-[(1-methylpiperidin-4-yl)methoxy]quinazolin-4-amine); vatalanib (PTK787, PTK/ZK, ZK222584) (N-(4-chlorophenyl)-4-(pyridin-4-ylmethyl)phthalazin-1-amine); AD-57 (N-[4-[4-amino-1-(1-methylethyl)-1H-pyrazolo[3,4-d]pyrimidin-3-yl]phenyl]-N′-[3-(trifluoromethyl)phenyl]-urea); AD-80 (1-[4-(4-amino-1-propan-2-ylpyrazolo[3,4-d]pyrimidin-3-yl) phenyl]-3-[2-fluoro-5-(trifluoromethyl) phenyl]urea); AD-81 (1-(4-(4-amino-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-3-yl)phenyl)-3-(4-chloro-3-(trifluoromethyl)phenyl)urea); ALW-II-41-27 (N-(5-((4-((4-ethylpiperazin-1-yl)methyl)-3-(trifluoromethyl) phenyl)carbamoyl)-2-methylphenyl)-5-(thiophen-2-yl)nicotinamide); BPR1K871 (1-(3-chlorophenyl)-3-(5-(2-((7-(3-(dimethylamino)propoxy)quinazolin-4-yl)amino)ethyl)thiazol-2-yl)urea); CLM3 (1-phenethyl-N-(1-phenylethyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine); EBI-907 (N-(2-chloro-3-(1-cyclopropyl-8-methoxy-3H-pyrazolo[3,4-c]isoquinolin-7-yl)-4-fluorophenyl)-3-fluoropropane-1-sulfonamide); NVP-AST-487 (N-[4-[(4-ethyl-1-piperazinyl)methyl]-3-(trifluoromethyl)phenyl]-N′-[4-[[6-(methylamino)-4-pyrimidinyl]oxy]phenyl]-urea); NVP-BBT594 (BBT594) (5-((6-acetamidopyrimidin-4-yl)oxy)-N-(4-((4-methylpiperazin-1-yl)methyl)-3-(trifluoromethyl)phenyl)indoline-1-carboxamide); PD173955 (6-(2,6-dichlorophenyl)-8-methyl-2-(3-methylsulfanylanilino)pyrido[2,3-d]pyrimidin-7-one); PP2 (4-amino-5-(4-chlorophenyl)-7-(dimethylethyl)pyrazolo[3,4-d]pyrimidine); PZ-1 (N-(5-(tert-butyl)isoxazol-3-yl)-2-(4-(5-(1-methyl-1H-pyrazol-4-yl)-1Hbenzo[d]imidazol-1-yl)phenyl)acetamide); RPI-1 (1,3-dihydro-5,6-dimethoxy-3-[(4-hydroxyphenyl)methylene]-H-indol-2-one; (3E)-3-[(4-hydroxyphenyl)methylidene]-5,6-dimethoxy-1H-indol-2-one); SGI-7079 (3-[2-[[3-fluoro-4-(4-methyl-1-piperazinyl)phenyl]amino]-5-methyl-7H-pyrrolo[2,3-d]pyrimidin-4-yl]-benzeneacetonitrile); SPP86 (1-Isopropyl-3-(phenylethynyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine); SU4984 (4-[4-[(E)-(2-oxo-1H-indol-3-ylidene)methyl]phenyl]piperazine-1-carbaldehyde); sunitinb (SU11248) (N-(2-Diethylaminoethyl)-5-[(Z)-(5-fluoro-2-oxo-1H-indol-3-ylidene)methyl]-2,4-dimethyl-1H-pyrrole-3-carboxamide); TG101209 (N-tert-butyl-3-(5-methyl-2-(4-(4-methylpiperazin-1-yl)phenylamino)pyrimidin-4-ylamino)benzenesulfonamide); Withaferin A ((4β,5β,6β,22R)-4,27-Dihydroxy-5,6:22,26-diepoxyergosta-2,24-diene-1,26-dione); XL-999 ((Z)-5-((1-ethylpiperidin-4-yl)amino)-3-((3-fluorophenyl) (5-methyl-1H-imidazol-2-yl)methylene) indolin-2-one); BPR1J373 (a 5-phenylthiazol-2-ylamine-pyriminide derivative); CG-806 (CG′806); DCC-2157; GTX-186; HG-6-63-01 ((E)-3-(2-(4-chloro-1H-pyrrolo[2,3-b]pyridin-5-yl)vinyl)-N-(4-((4-ethylpiperazin-1-yl)methyl)-3-(trifluoromethyl)phenyl)-4-methylbenzamide); SW-01 (Cyclobenzaprine hydrochloride); XMD15-44 (N-(4-((4-ethylpiperazin-1-yl)methyl)-3-(trifluoromethyl)phenyl)-4-methyl-3-(pyridin-3-ylethynyl)benzamide (generated from structure)); Y078-DM1 (an antibody drug conjugate composed of a RET antibody (Y078) linked to a derivative of the cytotoxic agent maytansine); Y078-DM4 (an antibody drug conjugate composed of a RET antibody (Y078) linked to a derivative of the cytotoxic agent maytansine); ITRI-305 (DON5 TB, DIB003599); BLU-667; BLU6864; DS-5010; GSK3179106; GSK3352589; and NMS-E668.

Further examples of RET-targeted therapeutics (e.g., a first RET kinase inhibitor or a second RET kinase inhibitor) include 5-amino-3-(5-cyclopropylisoxazol-3-yl)-1-isopropyl-1H-pyrazole-4-carboxamide; 3-(5-cyclopropylisoxazol-3-yl)-1-isopropyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine; 3-((6,7-Dimethoxyquinazolin-4-yl)amino)-4-fluoro-2-methylphenol; N-(5-(tert-butyl)isoxazol-3-yl)-2-(4-(imidazo[1,2-a]pyridin-6-yl)phenyl)acetamide; N-(5-(tert-butyl)isoxazol-3-yl)-2-(3-(imidazo[1,2-b]pyridazin-6-yloxy)phenyl)acetamide; N-(2-fluoro-5-trifluoromethylphenyl)-N′-{4′-[(2″-benzamido)pyridin-4″-ylamino]phenyl}urea; 2-amino-6-{[2-(4-chlorophenyl)-2-oxoethyl]sulfanyl}-4-(3-thienyl)pyridine-3,5-dicarbonitrile; and 3-arylureidobenzylidene-indolin-2-ones.

Additional examples of other RET kinase inhibitors include those described in U.S. Pat. Nos. 9,150,517 and 9,149,464, and International Publication No. WO 2014075035, all of which are hereby incorporated by reference. For example, in some embodiments the other RET inhibitor is a compound of formula I:

wherein R₁ is C₆-C₂₄alkyl or polyethylene glycol; or a pharmaceutically acceptable salt form thereof. In some embodiments, the other RET inhibitor is 4-{5-[bis-(chloroethyl)-amino]-1-methyl-1H-benzimidazol-2-yl}butyric acid dodecyl ester.

Additional examples of other RET kinase inhibitors include those described in International Publication No. WO 2016127074, which is hereby incorporated by reference. For example, in some embodiments, the other RET inhibitor is a compound of Formula (I) or a pharmaceutically acceptable salt thereof, wherein:

wherein Rings A and B are each independently selected from aryl, heteroaryl, cycloalkyl and heterocyclyl;

each L¹ and L² is independently selected from a bond, —(C1-C6 alkylene)-, —(C2-C6alkenylene)-, —(C2-C6 alkynylene)-, —(C1-C6 haloalkylene)-, —(C1-C6 heteroalkylene)-, —C(O)—, —O—, —S—, —S(O), —S(O)₂—, —N(R¹)—, —O—(C1-C6 alkylene)-, —(C1-C6 alkylene)-O—, —N(R¹)—C(O)—, —C(O)N(R¹)—, —(C1-C6 alkylene)-N(R¹)—, —N(R¹)—(C1-C6 alkylene)-, —N(R¹)—C(O)—(C1-C6 alkylene)-, —(C1-C6 alkylene)-N(R¹)—C(O)—, —C(O)—N(R¹)—(C1-C6 alkylene)-, —(C1-C6 alkylene)-C(O)—N(R¹)—, —N(R¹)—S(O)₂—, —S(O)₂—N(R¹)—, —N(R¹)—S(O)₂—(C1-C6 alkylene)-, and —S(O)₂—N(R¹)—(C1-C6 alkylene)-; wherein each alkylene, alkenylene, alkynylene, haloalkylene, and heteroalkylene is independently substituted with 0-5 occurrences of R′;

each R^(A) and R^(B) is independently selected from C1-C6 alkyl, C1-C6 alkoxy, halo, C1-C6 haloalkyl, C1-C6 hydroxyalkyl, C1-C6 heteroalkyl, and —N(R¹)(R¹); wherein each alkyl, alkoxy, haloalkyl, hydroxyalkyl, and hydroxyalkyl is independently substituted with 0-5 occurrences of R^(a);

each R^(C) and R^(D) is independently selected from C1-C6 alkyl, C2-C6 alkenyl, C2-C6 alkynyl, C1-C6 alkoxy, halo, C1-C6 heteroalkyl, C1-C6 haloalkyl, C1-C6 haloalkoxy, C1-C6 hydroxyalkyl, cycloalkyl, aryl, heteroaryl, aryloxy, aralkyl, heterocyclyl, heterocyclylalkyl, nitro, cyano, —C(O)R¹, —OC(O)R¹, —C(O)OR¹, —(C1-C6 alkylene)-C(O)R¹, —SR¹, —S(O)₂R¹, —S(O)₂—N(R¹)(R¹), —(C1-C6 alkylene)-S(O)₂R¹, —(C1-C6 alkylene)-S(O)₂—N(R¹)(R¹), —N(R¹)(R¹)—C(O)—N(R¹)(R¹)—N(R¹)—C(O)R¹, —N(R¹)—C(O)OR¹, —(C1-C6 alkylene)-N(R¹)—C(O)R¹, —N(R¹)S(O)₂R¹, and —P(O)(R¹)(R¹); wherein each of alkyl, alkenyl, alkynyl, alkoxy, heteroalkyl, haloalkyl, haloalkoxy, hydroxyalkyl, cycloalkyl, aryl, heteroaryl, aryloxy, aralkyl, heterocyclyl, and heterocyclylalkyl is independently substituted with 0-5 occurrences of R^(a); or 2 R^(C) or 2 R^(D) together with the carbon atom(s) to which they are attached form a cycloalkyl or heterocyclyl ring independently substituted with 0-5 occurrences of R^(a);

each R¹ is independently selected from hydrogen, hydroxyl, halo, thiol, C1-C6 alkyl, C1-C6 thioalkyl, C1-C6 alkoxy, C1-C6 haloalkyl, C1-C6 hydroxyalkyl, C1-C6 heteroalkyl, cycloalkyl, cycloalkylalkyl, heteroarylalkyl, heterocyclyl, and heterocyclylalkyl, wherein each of alkyl, thioalkyl, alkoxy, haloalkyl, hydroxyalkyl, heteroalkyl, cycloalkyl, cycloalkylalkyl, heteroarylalkyl, heterocyclyl, and heterocyclylalkyl is independently substituted with 0-5 occurrences of R^(b), or 2 R¹ together with the atom(s) to which they are attached form a cycloalkyl or heterocyclyl ring independently substituted with 0-5 occurrences of R^(b);

each R^(a) and R^(b) is independently C1-C6 alkyl, halo, hydroxyl, C1-C6 haloalkyl, C1-C6 heteroalkyl, C1-C6 hydroxyalkyl, C1-C6 alkoxy, cycloalkyl, heterocyclyl, or cyano, wherein each of alkyl, haloalkyl, heteroalkyl, hydroxyalkyl, alkoxy, cycloalkyl and heterocyclyl is independently substituted with 0-5 occurrences of R′;

each R′ is C1-C6 alkyl, C1-C6 heteroalkyl, halo, hydroxyl, C1-C6 haloalkyl, C1-C6 hydroxyalkyl, cycloalkyl or cyano; or 2 R′, together with the atom(s) to which they are attached form a cycloalkyl or heterocyclyl ring;

m is 0, 1, 2, or 3;

n is 0, 1, or 2; and

p and q are each independently 0, 1, 2, 3, or 4. For example, a RET inhibitor can be selected from the group consisting of:

or a pharmaceutically acceptable salt thereof.

Additional examples of other RET kinase inhibitors include those described in International Publication No. WO 2016075224, which is hereby incorporated by reference. For example, in some embodiments, the other RET inhibitor is a compound of Formula (II) or a pharmaceutically acceptable salt thereof, wherein:

R¹ and R² are independently hydrogen or an optionally substituted group selected from straight or branched (C₁-C₆) alkyl, (C₃-C₆) cycloalkyl and COR′, wherein R′ is an optionally substituted group selected from straight or branched (C₁-C₆) alkyl and (C₃-C₆) cycloalkyl;

R³ is hydrogen or an optionally substituted group selected from straight or branched (C₁-C₆) alkyl, (C₂-C₆) alkenyl, (C₂-C₆) alkynyl, (C₃-C₆) cycloalkyl, aryl, heteroaryl and a 3- to 7-membered heterocyclyl ring;

R⁴ is hydrogen or an optionally substituted group selected from straight or branched (C₁-C₆) alkyl, (C₂-C₆) alkenyl, aryl, heteroaryl or heterocyclyl;

A is a 5- or 6-membered heteroaryl ring or a phenyl ring;

B is a 5- or 6-membered ring selected from heteroaryl, (C₅-C₆) cycloalkyl and heterocyclyl ring or a phenyl ring; wherein ring A and ring B are fused together to form a bicyclic system comprising a 6-membered aromatic or 5- to 6-membered heteroaromatic ring fused with a 6-membered aromatic or 5- to 6-membered heteroaromatic, (C₅-C₆) cycloalkyl or heterocyclyl ring;

Y is carbon or nitrogen;

X is hydrogen, halogen, hydroxyl, cyano or an optionally substituted group selected from straight or branched (C₁-C₆) alkyl and (C₁-C₆) alkoxyl; and

R5 and R6 are independently hydrogen or an optionally substituted group selected from straight or branched (C₁-C₆) alkyl, (C₃-C₆) cycloalkyl, heterocyclyl, aryl and heteroaryl.

Additional examples of other RET kinase inhibitors include those described in International Publication No. WO 2015079251, which is hereby incorporated by reference. For example, in some embodiments, the other RET inhibitor is a compound of Formula (III) or a pharmaceutically acceptable salt or solvate thereof, wherein:

X is NH, NR_(x), O or S, wherein R_(x) is (1-3C)alkyl;

R₁ is selected from halo (e.g., fluoro, chloro, or bromo), trifluoromethyl, (1-4C)alkyl (e.g., methyl), (1-4C)alkoxy or (3-6C)cycloalkyl, wherein an alkyl, alkoxy or cycloalkyl group is optionally substituted with one or more fluoro;

R₂ is selected from hydrogen, halo (e.g., fluoro, chloro or bromo), hydroxyl, cyano, trifluoromethyl, trifluoromethoxy, (1-6C)alkyl (e.g., methyl), (3-8C)cycloalkyl, or (1-4C)alkoxy (e.g., OMe), wherein an alkyl, cycloalkyl or alkoxy group is optionally substituted with one or more fluoro;

R₃ is selected from hydrogen, halo (e.g. fluoro, chloro or bromo), hydroxyl, cyano, trifluoromethyl, trifluoromethoxy, (1-6C)alkyl (e.g., methyl), (3-8C)cycloalkyl, or (1-4C)alkoxy (e.g., OMe), wherein an alkyl, cycloalkyl or alkoxy group is optionally substituted with one or more fluoro;

R₄ is selected from hydrogen, halo (e.g., fluoro, chloro or bromo), hydroxyl, cyano, trifluoromethyl, trifluoromethoxy, (1-6C)alkyl (e.g., methyl), (3-8C)cycloalkyl, or (1-4C)alkoxy (e.g., OMe), wherein an alkyl, cycloalkyl or alkoxy group is optionally substituted with one or more fluoro;

R₅ is selected from hydrogen or a group defined by the formula: —O-L₅-X₅-Q₅;

wherein

-   -   L₅ is absent or a linear or branched (1-4C)alkylene;     -   X₅ is absent or —C(O)O—, —O—, —C(O)—, —OC(O)—, —CH(QR_(5L))—,         —N(R^(j))—, —N(R_(5L))—C(O)—, —N(R_(5L))—C(O)O—,         —C(O)—N(R_(5L))—, —S—, —SO—, —SO₂—, —S(O)₂N(R_(5L))—, or         —N(R_(5L))SO₂— wherein R_(5L) is selected from hydrogen or         methyl; and     -   Q₅ is (1-6C)alkyl, (2-6C)alkenyl, (2-6C)alkynyl,         (3-8C)cycloalkyl, (3-8C)cycloalkyl-(1-4C)alkyl, aryl,         aryl-(1-4C)alkyl, heteroaryl, heteroaryl-(1-4C)alkyl,         heterocyclyl or heterocyclyl-(1-4C)alkyl;

R₆ is selected from hydrogen, or a group defined by the formula: —O-L₆-X₆-Q₆

wherein

-   -   L₆ is absent or a linear or branched (1-4C)alkylene;     -   X₆ is absent or selected from —O—, —C(O)—, —C(O)O—, —OC(O)—,         —CH(OR_(6L))—, —N(R_(6L)), —N(R_(6L))—C(O)—, —N(R_(6L))—C(O)O—,         —C(O)—N(R_(6L))—, —S—, —SO—, —SO₂—, —S(O)₂N(R_(6L))—, or         —N(R_(6L))SO₂— wherein R^(6L) is selected from hydrogen or         (1-3C)alkyl;     -   Q₆ is hydrogen, (1-8C)alkyl, (2-8C)alkenyl, (2-8C)alkynyl,         (3-8C)cycloalkyl, (3-8C)cycloalkyl-(1-6C)alkyl, aryl,         aryl-(1-6C)alkyl, heteroaryl, heteroaryl-(1-6C)alkyl,         heterocyclyl, heterocyclyl-(1-6C)alkyl,     -   or Q₆ and R_(L6) are linked such that, together with the         nitrogen atom to which they are attached, they form a         heterocyclic ring;     -   wherein R₆ is optionally substituted (e.g. substituted on L₆         and/or Q₆) with one or more (1-6C)alkyl, (1-6C)alkanoyl,         OR_(6X), SR_(6X), S(O)R_(6X), S(O)₂R_(6X), C(O)OR_(6X) or         C(O)NR_(6X)R′_(6X), wherein R_(6X) and R′_(6X) are independently         hydrogen, (1-8C)alkyl, or R_(6X) and R′_(6X) are linked such         that, together with the nitrogen atom to which they are         attached, they form a heterocyclic ring; and

R₇ is selected from hydrogen, (1-6C)alkoxy, or a group defined by the formula: —O-L₇-X₇-Q₇-

wherein

-   -   L₇ is absent or a linear or branched (1-4C)alkylene;     -   X₇ is absent or selected from —O—, —C(O)—, —C(O)O—, —OC(O)—,         —CH(OR_(6L))—, —N(R_(7L))—, —N(R_(7L))—C(O)—, —N(R_(7L))—C(O)O—,         —C(O)—N(R_(7L))—, —S—, —SO—, —SO₂—, —S(O)₂N(R_(7L))—, or         —N(R_(7L))SO₂— wherein R_(7L) is selected from hydrogen or         (1-3C)alkyl;     -   Q₇ is hydrogen, (1-8C)alkyl, (2-8C)alkenyl, (2-8C)alkynyl,         (3-8C)cycloalkyl, (3-8C)cycloalkyl-(1-6C)alkyl, aryl,         aryl-(1-6C)alkyl, heteroaryl, heteroaryl-(1-6C)alkyl,         heterocyclyl, heterocyclyl-(1-6C)alkyl,     -   or Q₇ and R_(7L) are linked such that, together with the         nitrogen atom to which they are attached, they form a         heterocyclic ring;     -   wherein R₇ is optionally substituted (e.g., substituted on L₇         and/or Q₇) with one or more halo, hydroxyl, nitro, cyano,         (1-8C)alkyl, (1-8C)alkanoyl, OR_(7X), SR_(7X), S(O)R_(7X),         S(O)₂R_(7X), C(O)OR_(7X) or C(O)NR_(7X)R′_(7X), wherein R_(7X)         and R′_(7X) are independently hydrogen, (1-8C)alkyl, or R_(7X)         and R′_(7X) are linked such that, together with the nitrogen         atom to which they are attached, they form a heterocyclic ring;         or     -   R₇ is optionally substituted with one or more groups selected         from oxo, (1-4C)haloalkyl, (1-4C)hydroxyalkyl, C(O)R_(7y) or         NR_(7y)R′_(7y), wherein R_(7y) and R′_(7y) are independently         hydrogen or (1-8C)alkyl.

Additional examples of other RET kinase inhibitors include those described in International Publication No. WO2017178845, which is hereby incorporated by reference. For example, in some embodiments, the other RET inhibitor is a compound of Formula (IV) or a pharmaceutically acceptable salt thereof, wherein:

HET is selected from one of the following:

wherein

denotes the point of attachment;

R₁ is selected from hydrogen, (1-4C)haloalkyl, (1-4C)haloalkoxy or a group of the formula: -L-Y-Q

wherein:

-   -   L is absent or (1-5C)alkylene optionally substituted by one or         more substituents selected from (1-2C)alkyl or oxo;     -   Y is absent or O, S, SO, SO₂, N(R_(a)), C(O), C(O)O, OC(O),         C(O)N(R_(a)), N(R_(a))C(O), N(R_(a))C(O)N(R_(b)), N(R_(a))C(O)O,         OC(O)N(R_(a)), S(O)₂N(R_(a)), or N(R_(a))SO₂, wherein R_(a) and         R_(b) are each independently selected from hydrogen or         (1-4C)alkyl; and     -   Q is hydrogen, (1-6C)alkyl, (2-6C)alkenyl, (2-6C)alkynyl, aryl,         (3-10C)cycloalkyl, (3-10C)cycloalkenyl, heteroaryl or         heterocyclyl; wherein Q is optionally further substituted by one         or more substituent groups independently selected from         (1-4C)alkyl, halo, (1-4C)haloalkyl, (1-4C)haloalkoxy, amino,         (1-4C)aminoalkyl, cyano, hydroxy, carboxy, carbamoyl,         sulphamoyl, mercapto, ureido, NR_(c)R_(d), OR_(c), C(O)R_(c),         C(O)OR_(c), OC(O)R_(c), C(O)N(R_(d))R_(c), N(R_(d))C(O)R_(c),         S(O)_(p)R_(c) (where p is 0, 1 or 2), SO₂N(R_(d))R_(c),         N(R_(d))SO₂R_(c), Si(R_(e))(R_(d))R_(c) or (CH₂)_(q)NR_(c)R_(d)         (where q is 1, 2 or 3); wherein R_(c), R_(d) and R_(e) are each         independently selected from hydrogen, (1-6C)alkyl or         (3-6C)cycloalkyl; or R_(c) and R_(d) are linked such that,         together with the nitrogen atom to which they are attached, they         form a 4-7 membered heterocyclic ring which is optionally         substituted by one or more substituents selected from         (1-4C)alkyl, halo, (1-4C)haloalkyl, (1-4C)haloalkoxy,         (1-4C)alkoxy, (1-4C)alkylamino, amino, cyano or hydroxy; or

Q is optionally substituted by a group of the formula: -L₁-L_(Q1)-W₁

wherein:

-   -   L₁ is absent or (1-3C)alkylene optionally substituted by one or         more substituents selected from (1-2C)alkyl or oxo;     -   L_(Q1) is absent or selected from O, S, SO, SO₂, N(R_(f)), C(O),         C(O)O, OC(O), C(O)N(R_(f)), N(R_(f))C(O), N(R_(f))C(O)N(R_(g)),         N(R_(f))C(O)O, OC(O)N(R_(f)), S(O)₂N(R_(f)), or N(R_(f))SO₂,         wherein R_(f) and R_(g) are each independently selected from         hydrogen or (1-2C)alkyl; and     -   W₁ is hydrogen, (1-6C)alkyl, aryl, aryl(1-2C)alkyl,         (3-8C)cycloalkyl, (3-8C)cycloalkenyl, heteroaryl or         heterocyclyl; wherein W₁ is optionally substituted by one or         more substituents selected from (1-4C)alkyl, halo,         (1-4C)haloalkyl, (1-4C)haloalkoxy, (1-4C)alkoxy,         (1-4C)alkylamino, amino, cyano, hydroxy, carboxy, carbamoyl,         sulphamoyl, mercapto, ureido, aryl, heteroaryl, heterocycyl,         (3-6C)cycloalkyl, NR_(h)R_(i), OR_(h), C(O)R_(h), C(O)OR_(h),         OC(O)R_(h), C(O)N(R_(i))R_(h), N(R_(i))C(O)R_(h), S(O)_(r)R_(h)         (where r is 0, 1 or 2), SO₂N(R_(i))R_(h), N(R_(i))SO₂R_(h) or         (CH₂)_(s)NR_(i)R_(h) (where s is 1, 2 or 3); wherein R_(h) and         R_(i) are each independently selected from hydrogen, (1-4C)alkyl         or (3-6C)cycloalkyl;

R_(1a) and R_(1b) are each selected from H, (1-4C)alkyl, halo, (1-4C)haloalkyl, (1-4C)haloalkoxy, (1-4C)alkoxy, (1-4C)alkylamino, amino, cyano, hydroxy, carboxy, carbamoyl, sulphamoyl or mercapto;

W is selected from 0, S or NR_(W1), wherein R_(W1) is selected from H or (1-2C)alkyl;

X¹, X₂, X₃ and X₄ are independently selected from CH, CR₂ or N;

R₂ is selected from hydrogen, halo, (1-4C)alkyl, (1-4C)alkoxy, (1-4C)haloalkyl, (1-4C)haloalkoxy, amino, cyano, nitro, aryl, heteroaryl, heterocyclyl, cycloalkyl, (2-4C)alkynyl, NR_(j)R_(k), OR_(j), C(O)R_(j), C(O)OR_(j), OC(O)R_(j), C(O)N(R_(k))R_(j), N(R_(k))C(O)R_(j), N(R_(k))C(O)N(R_(j)), S(O)_(r1)R_(k) (where r₁ is 0, 1 or 2), SO₂N(R_(j))R_(k), N(R^(j))SO₂R_(k) or (CH₂)_(v)NR_(j)R_(k) (where v is 1, 2 or 3); wherein R_(j) and R_(k) are each independently selected from hydrogen or (1-4C)alkyl; and wherein said (1-4C)alkyl, aryl, heteroaryl, heterocycyl or cycloalkyl is optionally substituted by one or more substituents selected from halo, (1-4C)alkyl, (1-4C)alkoxy, (1-4C)haloalkyl, (1-4C)haloalkoxy, amino, cyano, nitro, phenyl, (2-4C)alkynyl, NR_(j1)R_(k1), OR_(j1), C(O)R_(j1), C(O)OR_(j1), OC(O)R_(j1), C(O)N(R_(k1))R_(j1), N(R_(k1))C(O)R_(j1), S(O)_(r2)R_(h) (where r₂ is 0, 1 or 2), SO₂N(R_(j1))R_(k1), N(R_(j1))SO₂R_(k1) or (CH₂)_(v1)NR_(j1)R_(k1) (where v₁ is 1, 2 or 3); and wherein R_(j1) and R_(k1) are each independently selected from hydrogen or (1-4C)alkyl; and

R₃ is selected from halo, (1-4C)alkyl, (1-4C)alkoxy, (1-4C)haloalkyl, (1-4C)haloalkoxy, amino, cyano, nitro, (2-4C)alkynyl, NR_(l)R_(m), OR_(l), C(O)R_(l), C(O)OR_(l), OC(O)R_(l), C(O)N(R_(m))R_(l), N(R_(m))C(O)R_(l), or (CH₂)_(y)NR_(l)R_(m) (where y is 1, 2 or 3); wherein said (1-4C)alkyl is optionally substituted by one or more substituents selected from amino, hydroxy, (1-2C)alkoxy or halo; and wherein R_(l) and R_(m) are each independently selected from hydrogen or (1-4C)alkyl.

Additional examples of other RET kinase inhibitors include those described in International Publication No. WO2017178844, which is hereby incorporated by reference. For example, in some embodiments, the other RET inhibitor is a compound of Formula (V) or a pharmaceutically acceptable salt thereof, wherein:

HET is selected from one of the following:

wherein

denotes the point of attachment;

R₁ is selected from hydrogen, (1-4C)haloalkyl, (1-4C)haloalkoxy or a group of the formula: -L-Y-Q

wherein:

-   -   L is absent or (1-5C)alkylene optionally substituted by one or         more substituents selected from (1-2C)alkyl or oxo;     -   Y is absent or O, S, SO, SO₂, N(R_(a)), C(O), C(O)O, OC(O),         C(O)N(R_(a)), N(R_(a))C(O), N(R_(a))C(O)N(R_(b)), N(R_(a))C(O)O,         OC(O)N(R_(a)), S(O)₂N(R_(a)), or N(R_(a))SO₂, wherein R_(a) and         R_(b) are each independently selected from hydrogen or         (1-4C)alkyl; and     -   Q is hydrogen, (1-6C)alkyl, (2-6C)alkenyl, (2-6C)alkynyl, aryl,         (3-10C)cycloalkyl, (3-10C)cycloalkenyl, heteroaryl or         heterocyclyl; wherein Q is optionally further substituted by one         or more substituent groups independently selected from         (1-4C)alkyl, halo, (1-4C)haloalkyl, (1-4C)haloalkoxy, amino,         (1-4C)aminoalkyl, cyano, hydroxy, carboxy, carbamoyl,         sulphamoyl, mercapto, ureido, NR_(c)R_(d), OR_(c), C(O)R_(c),         C(O)OR_(c), OC(O)R_(c), C(O)N(R_(d))R_(c), N(R_(d))C(O)R_(c),         S(O)_(y)R_(c) (where y is 0, 1 or 2), SO₂N(R_(d))R_(c),         N(R_(d))SO₂R_(e), Si(R_(d))(R_(c))R_(e) or (CH₂)_(z)NR_(c)R_(d)         (where z is 1, 2 or 3); wherein R_(c), R_(d) and R_(e) are each         independently selected from hydrogen, (1-6C)alkyl or         (3-6C)cycloalkyl; or R_(c) and R_(d) can be linked such that,         together with the nitrogen atom to which they are attached, they         form a 4-7 membered heterocyclic ring which is optionally         substituted by one or more substituents selected from         (1-4C)alkyl, halo, (1-4C)haloalkyl, (1-4C)haloalkoxy,         (1-4C)alkoxy, (1-4C)alkylamino, amino, cyano or hydroxyl; or     -   Q is optionally substituted by a group of the formula:         -L₁-L_(Q1)-Z₁     -   wherein:     -   L₁ is absent or (1-3C)alkylene optionally substituted by one or         more substituents selected from (1-2C)alkyl or oxo;     -   L_(Q1) is absent or selected from O, S, SO, SO₂, N(R_(f)), C(O),         C(O)O, OC(O), C(O)N(R_(f)), N(R_(f))C(O), N(R_(g))C(O)N(R_(f)),         N(R_(f))C(O)O, OC(O)N(R_(f)), S(O)₂N(R_(f)), or N(R_(f))SO₂,         wherein R_(f) and R_(g) are each independently selected from         hydrogen or (1-2C)alkyl; and     -   Z₁ is hydrogen, (1-6C)alkyl, aryl, aryl(1-2C)alkyl,         (3-8C)cycloalkyl, (3-8C)cycloalkenyl, heteroaryl or         heterocyclyl; wherein Z₁ is optionally substituted by one or         more substituents selected from (1-4C)alkyl, halo,         (1-4C)haloalkyl, (1-4C)haloalkoxy, (1-4C)alkoxy,         (1-4C)alkylamino, amino, cyano, hydroxy, carboxy, carbamoyl,         sulphamoyl, mercapto, ureido, aryl, heteroaryl, heterocycyl,         (3-6C)cycloalkyl, NR_(h)R_(i), OR_(h), C(O)R_(h), C(O)OR_(h),         OC(O)R_(h), C(O)N(R_(i))R_(h), N(R_(i))C(O)R_(h), S(O)_(ya)R_(h)         (where y^(a) is 0, 1 or 2), SO₂N(R_(i))R_(h), N(R_(i))SO₂R_(h)         or (CH₂)_(za)NR_(i)R_(h) (where z^(a) is 1, 2 or 3); wherein         R_(h) and R_(i) are each independently selected from hydrogen,         (1-4C)alkyl or (3-6C)cycloalkyl;

R_(1a) and R_(1b) are each selected from hydrogen, (1-4C)alkyl, halo, (1-4C)haloalkyl, (1-4C)haloalkoxy, (1-4C)alkoxy, (1-4C)alkylamino, amino, cyano, hydroxy, carboxy, carbamoyl, sulphamoyl or mercapto;

W is selected from O, So r NR_(j), wherein R_(j) is selected from H or (1-2C)alkyl;

X₁ and X₂ are each independently selected from N or CR_(k);

wherein

-   -   R_(k) is selected from hydrogen, halo, (1-4C)alkyl,         (1-4C)alkoxy, amino, (1-4C)alkylamino, (1-4C)dialkylamino,         cyano, (2C)alkynyl, C(O)R_(k1), C(O)OR_(k1), OC(O)R_(k1),         C(O)N(R_(k2))R_(k1), N(R_(k2))C(O)R_(k1), S(O)_(yb)R_(k1) (where         y^(b) is 0, 1 or 2), SO₂N(R_(k2))R_(k1), N(R_(k2))SO₂R_(k1) or         (CH₂)_(zb)NR_(k1)R_(k2) (where z^(b) is 1, 2 or 3); wherein said         (1-4C)alkyl is optionally substituted by one or more         substituents selected from amino, hydroxy, (1-2C)alkoxy or halo;         and     -   R_(k1) and R_(k2) are each independently selected from hydrogen         or (1-4C)alkyl;

X₃ is selected from N or CR_(m);

wherein

-   -   R_(m) is selected from hydrogen, halo, (1-4C)alkyl,         (1-4C)alkoxy, amino, (1-4C)alkylamino, (1-4C)dialkylamino,         cyano, (2C)alkynyl, C(O)R_(m1), C(O)OR_(m1), OC(O)R_(m1),         C(O)N(R_(m2))R_(m1), N(R_(m2))C(O)R_(m1), S(O)_(yc)R_(m1) (where         y^(c) is 0, 1 or 2), SO₂N(R_(m2))R_(m1), N(R_(m2))SO₂R_(m1) or         (CH₂)_(zc)NR_(m1)R_(m2) (where zc is 1, 2 or 3); wherein said         (1-4C)alkyl is optionally substituted by one or more         substituents selected from amino, hydroxy, (1-2C)alkoxy or halo;         and     -   R_(m1) and R_(m2) are each independently selected from hydrogen         or (1-4C)alkyl;

R_(o) is selected from halo, (1-4C)alkyl, (1-4C)alkoxy, amino, (1-4C)alkylamino, (1-4C)dialkylamino, cyano, (2C)alkynyl, C(O)R_(o1), C(O)OR_(o1), OC(O)R_(o1), C(O)N(R_(o2))R_(o1), N(R_(o2))C(O)R_(o1), S(O)_(yd)R_(o1) (where y^(d) is 0, 1 or 2), SO₂N(R_(o2))R_(o1), N(R_(o2))SO₂R_(o1) or (CH₂)_(zd)NR_(o1)R_(o2) (where z^(d) is 1, 2 or 3); wherein said (1-4C)alkyl is optionally substituted by one or more substituents selected from amino, hydroxy, (1-2C)alkoxy or halo; and

R_(o1) and R_(o2) are each independently selected from hydrogen or (1-4C)alkyl;

R₂ is selected from hydrogen, (1-4C)alkyl or a group of the formula: -L₂-Y₂-Q₂

wherein:

-   -   L₂ is absent or (1-3C)alkylene optionally substituted by one or         more substituents selected from (1-2C)alkyl or oxo;     -   Y₂ is absent or C(O), C(O)O, C(O)N(R_(p)), wherein R_(p) is         selected from hydrogen or (1-4C)alkyl; and     -   Q₂ is hydrogen, (1-6C)alkyl, aryl, (3-8C)cycloalkyl,         (3-8C)cycloalkenyl, heteroaryl or heterocyclyl; wherein Q₂ is         optionally further substituted by one or more substituent groups         independently selected from (1-4C)alkyl, halo, (1-4C)haloalkyl,         (1-4C)haloalkoxy, amino, cyano, hydroxy, carboxy, carbamoyl,         sulphamoyl, NR_(q)R_(r), OR_(q), wherein R_(q) and R_(r) are         each independently selected from hydrogen, (1-4C)alkyl or         (3-6C)cycloalkyl;

R₃ is selected from a group of the formula: —Y₃-Q₃

wherein:

-   -   Y₃ is C(O), C(O)N(R_(y)), C(O)N(R_(y))O, N(R_(y))(O)C, C(O)O,         OC(O), N(R_(y))C(O)N(R_(y1)), SO₂N(R_(y)), N(R_(y))SO₂,         oxazolyl, triazolyl, oxadiazolyl, thiazolyl, imidazolyl,         thiadiazolyl, pyridinyl, pyrazolyl, pyrrolyl or tetrazolyl,         wherein R_(y) and R_(y1) are independently selected from         hydrogen or (1-2C)alkyl; and     -   Q₃ is hydrogen, (1-6C)alkyl, aryl, aryl(1-2C)alkyl,         (3-8C)cycloalkyl, (3-8C)cycloalkenyl, heteroaryl or         heterocyclyl; wherein Q₃ is optionally further substituted by         one or more substituent groups independently selected from         (1-4C)alkyl, halo, (1-4C)haloalkyl, (1-4C)haloalkoxy, amino,         cyano, hydroxy, carboxy, carbamoyl, sulphamoyl, NR_(z)R_(aa),         OR_(z), wherein R_(z) and R_(aa) are each independently selected         from hydrogen, (1-4C)alkyl or (3-6C)cycloalkyl; or Q₃ is         optionally substituted by a group of the formula:         -L₄-LQ₄-Z₄     -   wherein:         -   L₄ is absent or (1-3C)alkylene optionally substituted by one             or more substituents selected from (1-2C)alkyl or oxo;         -   L_(Q4) is absent or selected from or O, S, SO, SO₂,             N(R_(ab)), C(O), C(O)O, OC(O), C(O)N(R_(ab)), N(R_(ab))C(O),             N(R_(ac))C(O)N(R_(ab)), N(R_(ab))C(O)O, OC(O)N(R_(ab)),             S(O)₂N(R_(ab)), or N(R_(ab))SO₂, wherein R_(ab) and R_(ac)             are each independently selected from hydrogen or             (1-2C)alkyl; and         -   Z₄ is hydrogen, (1-6C)alkyl, aryl, aryl(1-2C)alkyl,             (3-8C)cycloalkyl, (3-8C)cycloalkenyl, heteroaryl or             heterocyclyl; wherein Z₄ is optionally substituted by one or             more substituents selected from (1-4C)alkyl, halo,             (1-4C)haloalkyl, (1-4C)haloalkoxy, (1-4C)alkoxy,             (1-4C)alkylamino, amino, cyano, hydroxy, carboxy, carbamoyl,             sulphamoyl, mercapto, ureido, aryl, heteroaryl, heterocycyl,             (3-6C)cycloalkyl, NR_(ad)R_(ae), OR_(ad), C(O)R_(ad),             C(O)OR_(ad), OC(O)R_(ad), C(O)N(R_(ae))R_(ad),             N(R_(ae))C(O)R_(ad), S(O)_(ye)R_(ad) (where y^(e) is 0, 1 or             2), SO₂N(R_(ae))R_(ad), N(R_(ae))SO₂R_(ad) or             (CH₂)_(ze)NR_(ad)R_(ae) (where z^(e) is 1, 2 or 3); wherein             R_(a)a and R_(ae) are each independently selected from             hydrogen, (1-4C)alkyl or (3-6C)cycloalkyl; or         -   Q₃ and R_(y) are linked such that, together with the             nitrogen atom to which they are attached, they form a 4-7             membered heterocyclic ring which is optionally substituted             by one or more substituents selected from (1-4C)alkyl, halo,             (1-4C)haloalkyl, (1-4C)haloalkoxy, (1-4C)alkoxy,             (1-4C)alkylamino, amino, cyano or hydroxyl;

with the proviso that only one or two of X₁, X₂ or X₃ can be N.

Additional examples of other RET kinase inhibitors include those described in International Publication No. WO 2017145050, which is hereby incorporated by reference. For example, in some embodiments, the other RET has the Formula (VI) or is a pharmaceutically acceptable salt thereof.

Additional examples of other RET kinase inhibitors include those described in International Publication No. WO 2016038552 is hereby incorporated by reference. For example, in some embodiments, the other RET has the Formula (VII), or the Formula (VIII), or is a pharmaceutically acceptable salt thereof.

Yet other therapeutic agents include RET inhibitors such as those described, for example, in U.S. Pat. Nos. 9,738,660; 9,801,880; 9,682,083; 9,789,100; 9,550,772; 9,493,455; 9,758,508; 9,604,980; 9,321,772; 9,522,910; 9,669,028; 9,186,318; 8,933,230; 9,505,784; 8,754,209; 8,895,744; 8,629,135; 8,815,906; 8,354,526; 8,741,849; 8,461,161; 8,524,709; 8,129,374; 8,686,005; 9,006,256; 8,399,442; 7,795,273; 7,863,288; 7,465,726; 8,552,002; 8,067,434; 8,198,298; 8,106,069; 6,861,509; 8,299,057; 9,150,517; 9,149,464; 8,299,057; and 7,863,288; U.S. Publication Nos. 2018/0009817; 2018/0009818; 2017/0283404; 2017/0267661; 2017/0298074; 2017/0114032; 2016/0009709; 2015/0272958; 2015/0238477; 2015/0099721; 2014/0371219; 2014/0137274; 2013/0079343; 2012/0283261; 2012/0225057; 2012/0065233; 2013/0053370; 2012/0302567; 2011/0189167; 2016/0046636; 2013/0012703; 2011/0281841; 2011/0269739; 2012/0271048; 2012/0277424; 2011/0053934; 2011/0046370; 2010/0280012; 2012/0070410; 2010/0081675; 2010/0075916; 2011/0212053; 2009/0227556; 2009/0209496; 2009/0099167; 2010/0209488; 2009/0012045; 2013/0303518; 2008/0234267; 2008/0199426; 2010/0069395; 2009/0312321; 2010/0173954; 2011/0195072; 2010/0004239; 2007/0149523; 2017/0281632; 2017/0226100; 2017/0121312; 2017/0096425; 2017/0044106; 2015/0065468; 2009/0069360; 2008/0275054; 2007/0117800; 2008/0234284; 2008/0234276; 2009/0048249; 2010/0048540; 2008/0319005; 2009/0215761; 2008/0287427; 2006/0183900; 2005/0222171; 2005/0209195; 2008/0262021; 2008/0312192; 2009/0143399; 2009/0130229; 2007/0265274; 2004/0185547; and 2016/0176865; and International Publication Nos. WO 2017/145050; WO 2017/097697; WO 2017/049462; WO 2017/043550; WO 2017/027883; WO 2017/013160; WO 2017/009644; WO 2016/168992; WO 2016/137060; WO 2016/127074; WO 2016/075224; WO 2016/038552; WO 2015/079251; WO 2014/086284; WO 2013/042137; WO 2013/036232; WO 2013/016720; WO 2012/053606; WO 2012/047017; WO 2007/109045; WO 2009/042646; WO 2009/023978; WO 2009/017838; WO 2017/178845; WO 2017/178844; WO 2017/146116; WO 2017/026718; WO 2016/096709; WO 2007/057397; WO 2007/057399; WO 2007/054357; WO 2006/130613; WO 2006/089298; WO 2005/070431; WO 2003/020698; WO 2001/062273; WO 2001/016169; WO 1997/044356; WO 2007/087245; WO 2005/044835; WO 2014/075035; and WO 2016/038519; and J. Med. Chem. 2012, 55 (10), 4872-4876, all of which are hereby incorporated by reference in their entireties.

In some embodiments, a RET inhibitor (e.g., a first RET inhibitor or a second RET inhibitor) is a compound of the Formula II:

or a pharmaceutically acceptable salt or solvate thereof, wherein:

X¹ is CH, CCH₃, CF, CCl or N;

X² is CH, CF or N;

X³ is CH, CF or N;

X⁴ is CH, CF or N;

wherein zero, one or two of X¹, X², X³ and X⁴ is N;

A is H, Cl, CN, Br, CH₃, CH₂CH₃ or cyclopropyl;

B is hetAr¹;

hetAr¹ is a 5-membered heteroaryl ring having 1-3 ring heteroatoms independently selected from N, S and O, wherein said heteroaryl ring is optionally substituted with one or more substituents independently selected from the group consisting of halogen, C1-C6 alkyl, hydroxyC1-C6 alkyl, fluoroC1-C6 alkyl, difluoroC1-C6 alkyl, trifluoroC1-C6 alkyl, cyanoC1-C6 alkyl, (C1-C6 alkoxy)C1-C6 alkyl, (C1-C4 alkoxy)CH₂C(═O)—, (C1-C4 alkoxy)C(═O)C1-C3 alkyl, C3-C6 cycloalkyl, (R^(a)R^(b)N)C1-C6 alkyl, (R^(a)R^(b)N)C(═O)C1-C6 alkyl, (C1-C6 alkylSO₂)C1-C6 alkyl, hetCyc^(a), and 4-methoxybenzyl;

R^(a) and R^(b) are independently H or C1-C6 alkyl;

hetCyc^(a) is a 4-6 membered heterocyclic ring having a ring heteroatom selected from N and O, wherein said heterocyclic ring is optionally substituted with halogen, C1-C6 alkyl, fluoroC1-C6 alkyl, difluoroC1-C6 alkyl, trifluoroC1-C6 alkyl, (C1-C6 alkoxy)C1-C6 alkyl, di(C1-C3 alkyl)NCH₂C(═O), (C1-C6 alkoxy)C(═O) or (C1-C6 alkoxy)CH₂C(═O);

D is hetCyc¹, hetCyc², hetCyc³ or hetCyc⁹;

hetCyc¹ is a 4-6 membered heterocyclic ring having 1-2 ring atoms selected from N and O, wherein said heterocyclic ring is optionally substituted with one or more substituents independently selected from the group consisting of C1-C3 alkyl, fluoroC1-C3 alkyl, difluoroC1-C3 alkyl, trifluoroC1-C3 alkyl and OH, or said heterocyclic ring is substituted with a C3-C6 cycloalkylidene ring, or said heterocyclic ring is substituted with an oxo group;

hetCyc² is a 7-8 membered bridged heterocyclic ring having 1-3 ring heteroatoms independently selected from N and O, wherein said heterocyclic ring is optionally substituted with C1-C3 alkyl;

hetCyc³ is a 7-11 membered heterospirocyclic ring having 1-2 ring heteroatoms independently selected from N and O, wherein said ring is optionally substituted with C1-C3 alkyl;

hetCyc⁹ is a fused 9-10 membered heterocyclic ring having 1-3 ring nitrogen atoms and optionally substituted with oxo;

E is

-   -   (a) hydrogen,     -   (b) OH,     -   (c) R^(a)R^(b)N—, wherein R^(a) is H or C1-C6 alkyl and R^(b) is         H, C1-C6 alkyl or phenyl;     -   (d) C1-C6 alkyl optionally substituted with one to three         fluoros,     -   (e) hydroxyC1-C6 alkyl- optionally substituted with one to three         fluoros,     -   (f) C1-C6 alkoxy optionally substituted with one to three         fluoros,     -   (g) hydroxy(C1-C6 alkoxy) optionally substituted with one to         three fluoros,     -   (h) (C1-C6 alkoxy)hydroxy C1-C6 alkyl- optionally substituted         with one to three fluoros,     -   (i) (C1-C6 alkyl)C(═O)— optionally substituted with one to three         fluoros,     -   (j) (hydroxy C1-C6 alkyl)C(═O)— optionally substituted with one         to three fluoros,     -   (k) (C1-C6 alkoxy)C(═O)—,     -   (l) (C1-C6 alkoxy)(C1-C6 alkyl)C(═O)—,     -   (m) HC(═O)—,     -   (n) Cyc¹,     -   (o) Cyc¹C(═O)—,     -   (p) Cyc¹(C1-C6 alkyl)C(═O)— wherein said alkyl portion is         optionally substituted with one or more groups independently         selected from the group consisting of OH, fluoro, C1-C3 alkoxy         and R^(c)R^(d)N—, where R^(c) and R^(d) are independently H or         C1-C6 alkyl,     -   (q) hetCyc⁴,     -   (r) hetCyc⁴C(═O)—,     -   (s) hetCyc⁴(C1-C3 alkyl)C(═O)—,     -   (t) (hetCyc⁴)C(═O)C1-C2 alkyl-,     -   (u) hetCyc⁴C(═O)NH—,     -   (v) Ar²,     -   (w) Ar²C(═O)—,     -   (x) Ar²C1-C6 alkyl-,     -   (y) (Ar²)hydroxy C2-C6 alkyl-,     -   (z) Ar²(C1-C3 alkyl)C(═O)— wherein said alkyl portion is         optionally substituted with one or two groups independently         selected from the group consisting of OH, C1-C6 alkyl         (optionally substituted with 1-3 fluoros), hydroxyC1-C6 alkyl,         C1-C6 alkoxy and R^(e)R^(f)N—, where R^(e) and R^(f) are         independently H or C1-C6 alkyl, or R^(e) and R^(f) together with         the nitrogen to which they are attached form a 5-6 membered         azacyclic ring optionally having an additional ring heteroatom         selected from N and O,     -   (aa) hetAr²C(═O)—,     -   (bb) (hetAr²)hydroxyC2-C6 alkyl-,     -   (cc) hetAr²(C1-C3 alkyl)C(═O)—, wherein said alkyl portion is         optionally substituted with one or two groups independently         selected from the group consisting of OH, C1-C6 alkyl,         hydroxyC1-C6 alkyl, C1-C6 alkoxy and R^(e)R^(f)N—, wherein R^(e)         and R^(f) are independently H or C1-C6 alkyl or R^(e) and R^(f)         together with the nitrogen to which they are attached form a 5-6         membered azacyclic ring optionally having an additional ring         heteroatom selected from N and O,     -   (dd) R¹R²NC(═O)—,     -   (ee) R¹R²N(C1-C3 alkyl)C(═O)—, wherein said alkyl portion is         optionally substituted with phenyl,     -   (ff) R¹R²NC(═O)C1-C2 alkyl-,     -   (gg) R¹R²NC(═O)NH—,     -   (hh) CH₃SO₂(C1-C6 alkyl)C(═O)—,     -   (ii) (C1-C6 alkyl)SO₂—,     -   (jj) (C3-C6 cycloalkyl)CH₂SO₂—,     -   (kk) hetCyc⁵-SO₂—,     -   (ll) R⁴R⁵NSO₂—,     -   (mm) R⁶C(═O)NH—,     -   (nn) hetCyc⁶,     -   (oo) hetAr²C1-C6 alkyl-,     -   (pp) (hetCyc⁴)C1-C6 alkyl-,     -   (qq) (C1-C6 alkoxy)C1-C6 alkyl- optionally substituted with 1-3         fluoros,     -   (rr) (C3-C6 cycloalkoxy)C1-C6 alkyl-,     -   (ss) (C3-C6 cycloalkyl)C1-C6 alkyl-, wherein said cycloalkyl is         optionally substituted with 1-2 fluoros,     -   (tt) (R^(g)R^(h)N)C1-C6 alkyl-, wherein R^(g) and R^(h) are         independently H or C1-C6 alkyl,     -   (uu) Ar²—O—,     -   (vv) (C1-C6 alkylSO₂)C1-C6 alkyl-,     -   (ww) (C1-C6 alkoxy)C(═O)NHC1-C6 alkyl-,     -   (xx) (C3-C6 cycloalkoxy)C(═O)—,     -   (yy) (C3-C6 cycloalkyl)SO₂—, wherein said cycloalkyl is         optionally substituted with C1-C6 alkyl,     -   (zz) Ar⁴CH₂OC(═O)—,     -   (aaa) (N—(C1-C3 alkyl)pyridinonyl)C1-C3 alkyl-, and     -   (bbb) (Ar⁴SO₂)C1-C6 alkyl-;

Cyc¹ is a C3-C6 cycloalkyl, wherein (a) said cycloalkyl is optionally substituted with one or more substituents independently selected from the group consisting of OH, halogen, C1-C6 alkoxy, CN, hydroxyC1-C6 alkyl, (C1-C6 alkoxy)C1-C6 alkyl, and C1-C6 alkyl optionally substituted with 1-3 fluoros, or (b) said cycloalkyl is substituted with phenyl, wherein said phenyl is optionally substituted with one or more substituents independently selected from the group consisting of halogen, C1-C3 alkyl, C1-C3 alkoxy and CF, or (c) said cycloalkyl is substituted with a 5-6 membered heteroaryl ring having 1-3 ring heteroatoms independently selected from N and O, wherein said heteroaryl ring is optionally substituted with one or more substituents independently selected from the group consisting of halogen, C1-C3 alkyl, C1-C3 alkoxy and CF₃;

Ar² is phenyl optionally substituted with one or more substituents independently selected from the group consisting of halogen, C1-C6 alkyl, C1-C6 alkoxy (optionally substituted with 1-3 fluoros), fluoroC1-C6 alkyl, difluoroC1-C6 alkyl, trifluoroC1-C6 alkyl, CN, a 5-6 membered heterocyclic ring having 1-2 ring heteroatoms independently selected from N and O, and R^(i)R^(j)N— wherein R^(i) and R^(j) are independently H or C1-C6 alkyl;

hetAr² is a 5-6 membered heteroaryl ring having 1-3 ring heteroatoms independently selected from N, O and S and optionally substituted with one or more substituents independently selected from the group consisting of halogen, C1-C6 alkyl, C1-C6 alkoxy (optionally substituted with 1-3 fluoros), fluoroC1-C6 alkyl, difluoroC1-C6 alkyl, trifluoroC1-C6 alkyl, hydroxyC1-C6 alkyl, (C3-C6)cycloalkyl, (C1-C6 alkoxy)C1-C6 alkyl, CN, OH, and R′R″N—, wherein R′ and R″ are independently H or C1-C3 alkyl;

hetCyc⁴ is (a) a 4-6 membered heterocyclic ring having 1-2 ring heteroatoms independently selected from N, O and S wherein said S is optionally oxidized to SO₂, (b) a 7-8 membered bridged heterocyclic ring having 1-2 ring heteroatoms independently selected from N and O, (c) a 6-12 membered fused bicyclic heterocyclic ring having 1-2 ring heteroatoms independently selected from N and O and optionally independently substituted with 1-2 C1-C6 alkyl substitutents, or (d) a 7-10 membered spirocyclic heterocyclic ring having 1-2 ring heteroatoms independently selected from N and O, wherein each of said heterocyclic rings is optionally substituted with one or more substituents independently selected from the group consisting of halogen, OH, CN, C1-C6 alkyl (optionally substituted with 1-3 fluoros), C1-C6 alkoxy, (C1-C6 alkoxy)C1-C6 alkyl, (C3-C6)cycloalkyl, (C1-C6 alkyl)C(═O)—, a 5-6 membered heterocyclic ring having 1-2 ring heteroatoms independently selected from N and O, and phenyl wherein said phenyl is optionally substituted with one or more substituents selected from halogen, C1-C6 alkyl and C1-C6 alkoxy;

hetCyc⁵ is a 5-6 membered heterocyclic ring having a ring heteroatom selected from O and N;

hetCyc⁶ is a 5 membered heterocyclic ring having one or two ring heteroatoms independently selected from N and O, wherein said ring is substituted with oxo and wherein said ring is further optionally substituted with one or more substituents independently selected from the group consisting of OH and C1-C6 alkyl;

R¹ is H, C1-C6 alkyl or (C1-C6 alkoxy)C1-C6 alkyl;

R² is H, C1-C6 alkyl (optionally substituted with 1-3 fluoros), (C1-C6 alkoxy)C1-C6 alkyl (optionally substituted with 1-3 fluoros), Cyc³, hydroxyC1-C6 alkyl (optionally substituted with 1-3 fluoros), C1-C6 alkoxy (optionally substituted with 1-3 fluoros), (C1-C6 alkoxy)C(═O), hetCyc⁷, Ar³, Ar³C1-C3 alkyl-, hydroxyC1-C6 alkoxy or (3-6C cycloalkyl)CH₂O—;

Cyc³ is a 3-6 membered carbocyclic ring optionally substituted with 1-2 groups independently selected from the group consisting of C1-C6 alkoxy, OH and halogen;

hetCyc⁷ is a 5-6 membered heterocyclic ring having a ring heteroatom selected from O and N wherein said ring is optionally substituted with C1-C6 alkyl;

Ar³ is phenyl optionally substituted with one or more substituents independently selected from halogen, C1-C3 alkyl, C1-C3 alkoxy, fluoroC1-C3 alkyl, difluoroC1-C3 alkyl and trifluoroC1-C3 alkyl;

R⁴ and R⁵ are independently H or C1-C6 alkyl;

R⁶ is C1-C6 alkyl, hydroxyC1-C6 alkyl, C1-C6 alkoxy, (C1-C6 alkoxy)C1-C6 alkyl, phenyl or hetCyc⁸;

hetCyc⁸ is a 5-6 membered heterocyclic ring having a ring heteroatom selected from O and N, wherein said heterocyclic ring is optionally substituted with C1-C6 alkyl; and

Ar⁴ is phenyl optionally substituted with one or more halogens.

In some embodiments, a RET inhibitor (e.g., a first RET inhibitor or a second RET inhibitor) is a compound of the Formula III:

or a pharmaceutically acceptable salt or solvate thereof, wherein:

X¹ is CH or N;

X² is CH or N;

X³ is CH or N;

X⁴ is CH or N;

wherein one or two of X¹, X², X³ and X⁴ is N;

A is CN;

B is hetAr¹;

hetAr¹ is a 5-membered heteroaryl ring having 1-3 ring nitrogen atoms, wherein said heteroaryl ring is optionally substituted with one or more substituents independently selected from the group consisting of halogen, C1-C6 alkyl, hydroxyC1-C6 alkyl, fluoroC1-C6 alkyl, difluoroC1-C6 alkyl, trifluoroC1-C6 alkyl, cyanoC1-C6 alkyl, (C1-C6 alkoxy)C1-C6 alkyl, (C1-C4 alkoxy)CH₂C(═O)—, (C1-C4 alkoxy)C(═O)C1-C3 alkyl, C3-C6 cycloalkyl, (R′R^(b)N)C1-C6 alkyl, (R′R^(b)N)C(═O)C1-C6 alkyl, (C1-C6 alkylSO₂)C1-C6 alkyl, and 4-methoxybenzyl;

R^(a) and R^(b) are independently H or C1-C6 alkyl;

D is hetCyc¹;

hetCyc¹ is a 4-6 membered heterocyclic ring having 1-2 ring nitrogen atoms, wherein said heterocyclic ring is optionally substituted with one or more substituents independently selected from the group consisting of C1-C3 alkyl, fluoroC1-C3 alkyl, difluoroC1-C3 alkyl, trifluoroC1-C3 alkyl and OH, or said heterocyclic ring is substituted with a C3-C6 cycloalkylidene ring, or said heterocyclic ring is substituted with an oxo group;

E is

-   -   (w) Ar²C(═O)—,     -   (x) Ar²C1-C6 alkyl-,     -   (z) Ar²(C1-C3 alkyl)C(═O)— wherein said alkyl portion is         optionally substituted with one or two groups independently         selected from the group consisting of OH, C1-C6 alkyl         (optionally substituted with 1-3 fluoros), hydroxyC1-C6 alkyl,         C1-C6 alkoxy and R^(e)R^(f)N—, where R^(e) and R^(f) are         independently H or C1-C6 alkyl, or R^(e) and R^(f) together with         the nitrogen to which they are attached form a 5-6 membered         azacyclic ring optionally having an additional ring heteroatom         selected from N and O,     -   (cc) hetAr²(C1-C3 alkyl)C(═O)—, wherein said alkyl portion is         optionally substituted with one or two groups independently         selected from the group consisting of OH, C1-C6 alkyl,         hydroxyC1-C6 alkyl, C1-C6 alkoxy and R^(e)R^(f)N—, wherein R^(e)         and R^(f) are independently H or C1-C6 alkyl or R^(e) and R^(f)         together with the nitrogen to which they are attached form a 5-6         membered azacyclic ring optionally having an additional ring         heteroatom selected from N and O,     -   (dd) R¹R²NC(═O)—,     -   (oo) hetAr²C1-C6 alkyl-,

Ar² is phenyl optionally substituted with one or more substituents independently selected from the group consisting of halogen, C1-C6 alkyl, C1-C6 alkoxy (optionally substituted with 1-3 fluoros), fluoroC1-C6 alkyl, difluoroC1-C6 alkyl, trifluoroC1-C6 alkyl, CN, a 5-6 membered heterocyclic ring having 1-2 ring heteroatoms independently selected from N and O, and R^(i)R^(j)N— wherein R^(i) and R^(j) are independently H or C1-C6 alkyl;

hetAr² is a 5-6 membered heteroaryl ring having 1-3 ring heteroatoms independently selected from N, O and S and optionally substituted with one or more substituents independently selected from the group consisting of halogen, C1-C6 alkyl, C1-C6 alkoxy (optionally substituted with 1-3 fluoros), fluoroC1-C6 alkyl, difluoroC1-C6 alkyl, trifluoroC1-C6 alkyl, hydroxyC1-C6 alkyl, (C3-C6)cycloalkyl, (C1-C6 alkoxy)C1-C6 alkyl, CN, OH, and R′R″N—, wherein R′ and R″ are independently H or C1-C3 alkyl;

R¹ is H, C1-C6 alkyl or (C1-C6 alkoxy)C1-C6 alkyl; and

R² is H, C1-C6 alkyl (optionally substituted with 1-3 fluoros), (C1-C6 alkoxy)C1-C6 alkyl (optionally substituted with 1-3 fluoros), hydroxyC1-C6 alkyl (optionally substituted with 1-3 fluoros), C1-C6 alkoxy (optionally substituted with 1-3 fluoros), (C1-C6 alkoxy)C(═O), hydroxyC1-C6 alkoxy or (3-6C cycloalkyl)CH₂O.

In some embodiments, a RET inhibitor (e.g., a first RET inhibitor or a second RET inhibitor) is selected from the group consisting of: ((S)-4-(6-(4-(2-hydroxy-3-phenylpropanoyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(4-(2-(pyridin-2-yl)acetyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 4-(6-(4-(2,6-difluorobenzoyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile 2,2,2-trifluoroacetate; 4-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridin-4-yl)pyridin-2-yl)-N,N-diethylpiperazine-1-carboxamide; 1-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridin-4-yl)pyridin-2-yl)-N-(2-methoxy-3-methylbutyl)piperidine-4-carboxamide; 4-(6-(4-(2-(5-fluoropyridin-2-yl)acetyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile bis(2,2,2-trifluoroacetate); 4-(6-(4-(2,6-difluorobenzyl)piperazin-1-yl)pyridine-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 4-(6-(4-(2-methoxybenzyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(4-(pyridine-2-ylmethyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 4-(6-(4-((6-methoxypyridin-3-yl)methyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; or a pharmaceutically acceptable salt or solvate thereof.

In some embodiments, a RET inhibitor (e.g., a first RET inhibitor or a second RET inhibitor) is a compound of the Formula IV:

or a pharmaceutically acceptable salt or solvate thereof, wherein:

X¹, X², X³ and X⁴ are independently CH, CF, CCH₃ or N, wherein zero, one or two of X¹, X², X³ and X⁴ is N;

A is H, CN, Cl, CH₃—, CH₃CH₂—, cyclopropyl, —CH₂CN or —CH(CN)CH₃;

B is

-   -   (a) hydrogen,     -   (b) C1-C6 alkyl optionally substituted with 1-3 fluoros,     -   (c) hydroxyC2-C6 alkyl-, wherein the alkyl portion is optionally         substituted with 1-3 fluoros or a C3-C6 cycloalkylidene ring,     -   (d) dihydroxyC3-C6 alkyl-, wherein the alkyl portion is         optionally substituted with a C3-C6 cycloalkylidene ring,     -   (e) (C1-C6 alkoxy)C1-C6 alkyl- optionally substituted with 1-3         fluoros,     -   (f) (R¹R²N)C1-C6 alkyl- wherein said alkyl portion is optionally         substituted with OH and wherein R¹ and R² are independently H or         C1-C6 alkyl (optionally substituted with 1-3 fluoros);     -   (g) hetAr¹C1-C3 alkyl-, wherein hetAr¹ is a 5-6 membered         heteroaryl ring having 1-3 ring heteroatoms independently         selected from N, O and S and is optionally substituted with one         or more independently selected C1-C6 alkyl substituents;     -   (h) (C3-C6 cycloalkyl)C1-C3 alkyl-, wherein said cycloalkyl is         optionally substituted with OH,     -   (i) (hetCyc^(a))C1-C3 alkyl-,     -   (j) hetCyc^(a)-,     -   (k) C3-C6 cycloalkyl-, wherein said cycloalkyl is optionally         substituted with OH,     -   (l) (C1-C4 alkyl)C(═O)O—C1-C6 alkyl-, wherein each of the C1-C4         alkyl and C1-C6 alkyl portions is optionally and independently         substituted with 1-3 fluoros, or     -   (m) (R¹R²N)C(═O)C1-C6 alkyl-, wherein R¹ and R² are         independently H or C1-C6 alkyl (optionally substituted with 1-3         fluoros);

hetCyc^(a)- is a 4-6 membered heterocyclic ring having 1-2 ring heteroatoms independently selected from N and O and optionally substituted with one or more substituents independently selected from OH, C1-C6 alkyl (optionally substituted with 1-3 fluoros), hydroxyC1-C6 alkyl-, C1-C6 alkoxy, (C1-C6 alkyl)C(═O)—, (C1-C6 alkoxy)C1-C6 alkyl-, and fluoro, or wherein hetCyc^(a) is substituted with oxo;

Ring D is (i) a saturated 4-7 membered heterocyclic ring having two ring nitrogen atoms, (ii) a saturated 7-8 membered bridged heterocyclic ring having two ring nitrogen atoms and optionally having a third ring heteroatom which is oxygen, (iii) a saturated 7-11 membered heterospirocyclic ring having two ring nitrogen atoms, or (iv) a saturated 9-10 membered bicyclic fused heterocyclic ring having two ring nitrogen atoms, wherein each of said rings is optionally substituted with (a) one to four groups independently selected from halogen, OH, C1-C3 alkyl which is optionally substituted with 1-3 fluoros, or C1-C3 alkoxy which is optionally substituted with 1-3 fluoros, (b) a C3-C6 cycloalkylidene ring, or (c) an oxo group;

E is

-   -   (a) hydrogen,     -   (b) C1-C6 alkyl optionally substituted with 1-3 fluoros,     -   (c) (C1-C6 alkoxy)C1-C6 alkyl- optionally substituted with 1-3         fluoros,     -   (d) (C1-C6 alkyl)C(═O)—, wherein said alkyl portion is         optionally substituted with 1-3 fluoros or with a R^(g)R^(h)N—         substituent wherein R^(g) and R^(h) are independently H or C1-C6         alkyl,     -   (e) (hydroxyC2-C6 alkyl)C(═O)— optionally substituted with 1-3         fluoros,     -   (f) (C1-C6 alkoxy)C(═O)—,     -   (g) (C3-C6 cycloalkyl)C(═O)—, wherein said cycloalkyl is         optionally substituted with one or more substituents         independently selected from C1-C6 alkyl, C1-C6 alkoxy, OH, and         (C1-C6 alkoxy)C1-C6 alkyl-, or said cycloalkyl is substituted         with a 5-6 membered heteroaryl ring having 1-3 ring heteroatoms         independently selected from N and O,     -   (h) Ar¹C1-C6 alkyl-,     -   (i) Ar¹(C1-C6 alkyl)C(═O)—, wherein said alkyl portion is         optionally substituted with OH, hydroxyC1-C6 alkyl-, C1-C6         alkoxy, R^(m)R^(n)N— or R^(m)R^(n)N—CH₂—, wherein each R^(m) and         R^(n) is independently H or C1-C6 alkyl,     -   (j) hetAr²C1-C6 alkyl-, wherein said alkyl portion is optionally         substituted with 1-3 fluoros,     -   (k) hetAr²(C1-C6 alkyl)C(═O)— wherein said alkyl portion is         optionally substituted with OH, hydroxyC1-C6 alkyl- or C1-C6         alkoxy,     -   (l) hetAr²C(═O)—,     -   (m) hetCyc¹C(═O)—,     -   (n) hetCyc¹C1-C6 alkyl-,     -   (o) R³R⁴NC(═O)—,     -   (p) Ar¹N(R³)C(═O)—,     -   (q) hetAr²N(R³)C(═O)—,     -   (r) (C1-C6 alkyl)SO₂—, wherein the alkyl portion is optionally         substituted with 1-3 fluoros,     -   (s) Ar¹SO₂—,     -   (t) hetAr²SO₂—,     -   (u) N—(C1-C6 alkyl)pyridinonyl,     -   (v) Ar¹C(═O)—;     -   (w) Ar¹O—C(═O)—,     -   (x) (C3-C6 cycloalkyl)(C1-C6 alkyl)C(═O)—,     -   (y) (C3-C6 cycloalkyl)(C1-C6 alkyl)SO₂—, wherein the alkyl         portion is optionally substituted with 1-3 fluoros,     -   (z) Ar¹(C1-C6 alkyl)SO₂—,     -   (aa) hetCyc¹-O—C(═O)—,     -   (bb) hetCyc¹CH₂C(═O)—,     -   (cc) hetAr², or     -   (dd) C3-C6 cycloalkyl;

Ar¹ is phenyl optionally substituted with one or more substituents independently selected from the group consisting of halogen, CN, C1-C6 alkyl (optionally substituted with 1-3 fluoros), C1-C6 alkoxy (optionally substituted with 1-3 fluoros), R^(e)R^(f)N— wherein R^(e) and R^(f) are independently H, C1-C6 alkyl, (R^(p)R^(q)N)C1-C6 alkoxy- wherein R^(p) and R^(q) are independently H or C1-C6 alkyl, and (hetAr^(a))C1-C6 alkyl- wherein hetAr^(a) is a 5-6 membered heteroaryl ring having 1-2 ring nitrogen atoms, or Ar¹ is a phenyl ring fused to a 5-6 membered heterocyclic ring having 1-2 ring heteroatoms independently selected from N and O;

hetAr² is a 5-6 membered heteroaryl ring having 1-3 ring heteroatoms independently selected from N, O and S or a 9-10 membered bicyclic heteroaryl ring having 1-3 ring nitrogen atoms, wherein hetAr² is optionally substituted with one or more substituents independently selected from the group consisting of halogen, CN, C1-C6 alkyl (optionally substituted with 1-3 fluoros), C1-C6 alkoxy (optionally substituted with 1-3 fluoros), (C1-C6 alkoxy)C1-C6 alkyl- (optionally substituted with 1-3 fluoros), R^(e)R^(f)N— wherein R^(e) and R^(f) are independently H or C1-C6 alkyl, OH, (C1-C6 alkoxy)C1-C6 alkoxy- and C3-C6 cycloalkyl;

hetCyc¹ is a 4-6 membered saturated heterocyclic ring having 1-2 ring heteroatoms independently selected from N, O and S wherein said heterocyclic ring is optionally substituted with one or more substituents independently selected from C1-C6 alkoxy and halogen;

R³ is H or C1-C6 alkyl; and

R⁴ is C1-C6 alkyl.

In some embodiments, a RET inhibitor (e.g., a first RET inhibitor or a second RET inhibitor) is a compound of the Formula V:

or a pharmaceutically acceptable salt and solvate thereof, wherein:

X¹, X², X³ and X⁴ are independently CH or N, wherein zero, one or two of X¹, X², X³ and X⁴ is N;

A is CN;

B is

-   -   (b) C1-C6 alkyl optionally substituted with 1-3 fluoros,     -   (c) hydroxyC2-C6 alkyl-, wherein the alkyl portion is optionally         substituted with 1-3 fluoros or a C3-C6 cycloalkylidene ring,     -   (e) (C1-C6 alkoxy)C1-C6 alkyl- optionally substituted with 1-3         fluoros,     -   (f) (R¹R²N)C1-C6 alkyl-, wherein said alkyl portion is         optionally substituted with OH and wherein R¹ and R² are         independently H or C1-C6 alkyl (optionally substituted with 1-3         fluoros);     -   (g) hetAr¹C1-C3 alkyl-, wherein hetAr¹ is a 5-6 membered         heteroaryl ring having 1-3 ring heteroatoms independently         selected from N, O and S and is optionally substituted with one         or more independently selected C1-C6 alkyl substituents; or     -   (i) (hetCyc^(a))C1-C3 alkyl-,

hetCyc^(a)- is a 4-6 membered heterocyclic ring having 1-2 ring heteroatoms independently selected from N and O and optionally substituted with one or more substituents independently selected from OH, C1-C6 alkyl (optionally substituted with 1-3 fluoros), hydroxyC1-C6 alkyl-, C1-C6 alkoxy, (C1-C6 alkyl)C(═O)—, (C1-C6 alkoxy)C1-C6 alkyl- and fluoro, or wherein hetCyc^(a) is substituted with oxo;

Ring D is (i) a saturated 4-7 membered heterocyclic ring having two ring nitrogen atoms, or (ii) a saturated 7-9 membered bridged heterocyclic ring having two ring nitrogen atoms and optionally having a third ring heteroatom which is oxygen, wherein each of said rings is optionally substituted with (a) one to four groups independently selected from halogen, OH, C1-C3 alkyl which is optionally substituted with 1-3 fluoros, or C1-C3 alkoxy which is optionally substituted with 1-3 fluoros, (b) a C3-C6 cycloalkylidene ring, or (c) an oxo group;

E is

-   -   (h) Ar¹C1-C6 alkyl-,     -   (j) hetAr²C1-C6 alkyl-, wherein the alkyl portion is optionally         substituted with 1-3 fluoros, or     -   (l) hetAr²C(═O)—,

Ar¹ is phenyl optionally substituted with one or more substituents independently selected from the group consisting of halogen, CN, C1-C6 alkyl (optionally substituted with 1-3 fluoros), C1-C6 alkoxy (optionally substituted with 1-3 fluoros), R^(e)R^(f)N— wherein R^(e) and R^(f) are independently H or C1-C6 alkyl, (R^(p)R^(q)N)C1-C6 alkoxy- wherein R^(p) and R^(q) are independently H or C1-C6 alkyl, and (hetAr^(a))C1-C6 alkyl- wherein hetAr^(a) is a 5-6 membered heteroaryl ring having 1-2 ring nitrogen atoms, or Ar¹ is a phenyl ring fused to a 5-6 membered heterocyclic ring having 1-2 ring heteroatoms independently selected from N and O; and

hetAr² is a 5-6 membered heteroaryl ring having 1-3 ring heteroatoms independently selected from N, O and S or a 9-10 membered bicyclic heteroaryl ring having 1-3 ring nitrogen atoms, wherein hetAr² is optionally substituted with one or more substituents independently selected from the group consisting of halogen, CN, C1-C6 alkyl (optionally substituted with 1-3 fluoros), C1-C6 alkoxy (optionally substituted with 1-3 fluoros), (C1-C6 alkoxy)C1-C6 alkyl- (optionally substituted with 1-3 fluoros), R^(e)R^(f)N— wherein R^(e) and R^(f) are independently H or C1-C6 alkyl, OH, (C1-C6 alkoxy)C1-C6 alkoxy- and C3-C6 cycloalkyl.

In some embodiments, a RET inhibitor which is not a compound of Formula I is selected from the group consisting of: 4-(6-(4-benzylpiperazin-1-yl)pyridin-3-yl)-6-(2-morpholinoethoxy)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-hydroxyethoxy)-4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; (R)-6-(2-hydroxypropoxy)-4-(6-(4-((6-methoxypyridin-3-yl)methyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-hydroxy-2-methylpropoxy)-4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-methoxyethoxy)-4-(6-(4-((6-methoxypyridin-3-yl)methyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-hydroxy-2-methylpropoxy)-4-(6-(6-(6-methoxynicotinoyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-(dimethylamino)ethoxy)-4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)-6-(2-morpholinoethoxy)pyrazolo[1,5-a]pyridine-3-carbonitrile; 4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)-6-((1-methyl-1H-imidazol-4-yl)methoxy)pyrazolo[1,5-a]pyridine-3-carbonitrile; and 6-ethoxy-4-(5-(6-((5-fluoro-6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyrazin-2-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; or a pharmaceutically acceptable salt or solvate thereof.

In some embodiments, a RET inhibitor (e.g., a first RET inhibitor or a second RET inhibitor) is a compound of Formula VI:

or a pharmaceutically acceptable salt or solvate thereof, wherein:

X¹, X², X³ and X⁴ are independently CH, CCH₃, CF or N, wherein zero, one or two of X¹, X², X³ and X⁴ is N;

A is H, CN, Cl, methyl, ethyl or cyclopropyl;

B is:

-   -   (a) hydrogen,     -   (b) C1-C6 alkyl optionally substituted with 1-3 fluoros,     -   (c) hydroxyC2-C6 alkyl- wherein the alkyl portion is optionally         substituted with a C3-C6 cycloalkylidene ring,     -   (d) dihydroxyC3-C6 alkyl- wherein the alkyl portion is         optionally substituted with a C3-C6 cycloalkylidene ring,     -   (e) (C1-C6 alkoxy)C1-C6 alkyl- optionally substituted with 1-3         fluoros,     -   (f) (R¹R²N)C1-C6 alkyl- where R¹ and R² are independently         selected from H, C1-C6 alkyl (optionally substituted with 1-3         fluoros), (C1-C6 alkoxy)C1-C6 alkyl-, (C1-C6 alkyl)C(═O)— and         (C1-C6 alkoxy)C(═O)—;     -   (g) hetAr¹C1-C3 alkyl-, where hetAr¹ is a 5-6 membered         heteroaryl ring having 1-3 ring heteroatoms independently         selected from N, O and S and is optionally substituted with one         or more independently selected C1-C6 alkyl substituents;     -   (h) (C3-C6 cycloalkyl)C1-C3 alkyl-, wherein said cycloalkyl is         optionally substituted with OH,     -   (i) (hetCyc^(a))C1-C3 alkyl-,     -   (j) hetCyc^(a),     -   (k) (R¹R²N)C(═O)C1-C6 alkyl-, where R¹ and R² are independently         selected from H and C1-C6 alkyl;     -   (l) (R¹R²N)C(═O)—, where R¹ and R² are independently selected         from H and C1-C6 alkyl, or     -   (m) hetCyc^(a)C(═O)C1-C6 alkyl-;

hetCyc^(a) is a 4-6 membered heterocyclic ring having 1-2 ring heteroatoms independently selected from N and O and optionally substituted with one or more substituents independently selected from OH, C1-C6 alkyl (optionally substituted with 1-3 fluoros), hydroxyC1-C6 alkyl, halogen, (C1-C6 alkyl)C(═O)—, C1-C6 alkoxy, oxo and (C1-C6 alkoxy)C(═O)—;

Ring D is (i) a saturated monocyclic 4-7 membered heterocyclic ring having one ring heteroatom which is nitrogen, (ii) a saturated 7-8 membered bridged heterocyclic ring having one ring heteroatom which is nitrogen, or (iii) a saturated 7-11 membered heterospirocyclic ring system having one ring heteroatom which is nitrogen;

each R^(a) is independently C1-C6 alkyl (optionally substituted with 1-3 fluoros), hydroxyC1-C6 alkyl or (C1-C6 alkoxy)C1-C6 alkyl-;

R^(b) is (a) hydroxy, (b) cyclopropyl, (c) hetCyc^(b)CH₂—, (d) R^(i)R^(j)NC(═O)CH₂OCH₂— where R^(i) and R^(j) are independently H or C1-C6 alkyl, (e) R^(c)R^(d)N—, (f) R^(c)R^(d)NCH₂—, (g) C1-C6 alkoxy-, (h) (C1-C4 alkyl)-C(═O)NH— wherein said alkyl portion is optionally substituted with hetCyc^(b), hetAr^(a), C1-C6 alkoxy- or R′R″N—, or said alkyl portion is optionally substituted with two substituents independently selected from R′R″N— and OH, where each R′ and R″ is independently hydrogen or C1-C6 alkyl, (i) (R′R″N)C1-C6 alkoxy(CH₂)_(n)— where n is 0 or 1 and R′ and R″ are independently hydrogen or C1-C6 alkyl, (j) hetCyc^(b)(C1-C3 alkyl)OCH₂—, (k) hetCyc^(b)C(═O)NH— or (l) hetAr^(a)C(═O)NH—;

hetCyc^(b) is a 4-6 membered heterocyclic ring, a 7-8 membered bridged heterocyclic ring, or a 7-10 membered heterospirocyclic ring, each ring having 1-2 ring heteroatoms independently selected from N and O, wherein hetCyc^(b) is optionally substituted with one or more substituents independently selected from OH, fluoro, C1-C6 alkyl (optionally substituted with 1-3 fluoros), hydroxyC1-C6 alkyl- (optionally substituted with 1-3 fluoros), (C1-C6 alkoxy)C1-C6 alkyl-, (C1-C6 alkoxy)C(═O)—, C1-C6 alkoxy, and R′R″N— where R′ and R″ are independently hydrogen or C1-C6 alkyl;

hetAr^(a) is a 5-6 membered heteroaryl ring having 1-3 ring heteroatoms independently selected from N, O and S wherein hetAr^(a) is optionally substituted with one or more substituents independently selected from the group consisting of halogen, CN, C1-C6 alkyl (optionally substituted with 1-3 fluoros), and C1-C6 alkoxy (optionally substituted with 1-3 fluoros),

R^(c) is hydrogen or C1-C6 alkyl;

R^(d) is hydrogen, C1-C6 alkyl (optionally substituted with 1-3 fluoros), (C1-C6 alkoxy)C(═O)—, hydroxyC1-C6 alkyl (optionally substituted with 1-3 fluoros), (hydroxyC1-C6 alkyl)C(═O)—, (C1-C6 alkyl)C(═O)—, (R^(k)R^(l)N)C1-C6 alkyl- where R^(k) and R^(l) are independently H or C1-C6 alkyl, R^(m)R^(n)NC(═O)C1-C6 alkyl- where R^(m) and R^(n) are independently H or C1-C6 alkyl, PhCH₂— wherein the phenyl is optionally substituted with one or more substituents independently selected from the group consisting of halogen, CN, C1-C6 alkyl (optionally substituted with 1-3 fluoros), C1-C6 alkoxy (optionally substituted with 1-3 fluoros), (C1-C6 alkoxy)C1-C6 alkyl- (optionally substituted with 1-3 fluoros), C3-C6 cycloalkyl, hydroxyC1-C6 alkyl, (C1-C6 alkyl)SO₂—, R^(e)R^(f)N— and (R^(e)R^(f)N)C1-C6 alkyl- where each R^(e) and R^(f) is independently H or C1-C6 alkyl, (C1-C6 alkoxy)C1-C6 alkyl-, or hetCyc^(c) where hetCyc^(c) is a 4-6 membered heterocyclic ring having a ring heteroatom selected from N and O and optionally substituted with C1-C6 alkyl;

n is 0, 1, 2, 3, 4, 5 or 6;

m is 0 or 1;

E is:

-   -   (a) hydrogen,     -   (b) hydroxy,     -   (c) C1-C6 alkyl optionally substituted with 1-3 fluoros,     -   (d) Ar¹C1-C6 alkyl- wherein said alkyl portion is optionally         substituted with 1-3 fluoros,     -   (e) hetAr²C1-C6 alkyl-,     -   (f) (C1-C6 alkoxy)C1-C6 alkoxy-,     -   (g) Ar¹O—,     -   (h) hetAr²—O—,     -   (i) Ar¹NR^(g)— where R^(g) is H or C1-C6 alkyl,     -   (j) hetAr²NR^(g)— where R^(g) is H or C1-C6 alkyl,     -   (k) R³C(═O)NR^(g)— where R^(g) is H or C1-C6 alkyl;     -   (l) Ar¹C(═O)NR^(g)— where R^(g) is H or C1-C6 alkyl,     -   (m) hetAr²C(═O)NR^(g)(CH₂)_(p)— where p is 0 or 1 and R^(g) is H         or C1-C6 alkyl,     -   (n) R⁴R⁵NC(═O)—,     -   (o) Ar¹NR^(g)C(═O)—, where R^(g) is H or C1-C6 alkyl,     -   (p) hetAr²NR^(g)C(═O)—, where R^(g) is H or C1-C6 alkyl,     -   (q) Ar¹(C1-C6 alkyl)C(═O)— wherein said alkyl portion is         optionally substituted with OH, hydroxy(C1-C6 alkyl), C1-C6         alkoxy or NH₂,     -   (r) hetCyc⁵C(═O)—,     -   (s) R⁴R⁵NC(═O)NR^(g)— where R^(g) is H or C1-C6 alkyl, or     -   (t) (C1-C6 alkyl)SO₂—;     -   (u) Ar¹(C1-C6 alkyl)C(═O)NR^(g)— where R^(g) is H or C1-C6         alkyl,     -   (v) hetAr⁴C(═O)NR^(g)— where R^(g) is H or C1-C6 alkyl,     -   (w) hetAr²—S(═)—,     -   (x) (C3-C6 cycloalkyl)CH₂SO₂—,     -   (y) Ar¹(C1-C6 alkyl)SO₂—,     -   (z) hetAr²SO₂—,     -   (aa) Ar¹,     -   (bb) hetAr²,     -   (cc) hetCyc⁵,     -   (dd) C1-C6 alkoxy,     -   (ee) Ar¹(C1-C6 alkyl)-O—,     -   (ff) hetAr²(C1-C6 alkyl)-O—,     -   (gg) hetAr²—O—C1-C6 alkyl-,     -   (hh) Ar¹(C1-C6 alkyl)NR^(g)— where R^(g) is H or C1-C6 alkyl,     -   (ii) hetAr²—S—,     -   (jj) Ar²SO₂NR^(g)(CH₂)_(p)— where p is 0 or 1 and R^(g) is H or         C1-C6 alkyl,     -   (kk) (C1-C6 alkoxy)C(═O)—,     -   (ll) (C1-C6 alkyl)NR^(g)C(═O)O— where R^(g) is H or C1-C6 alkyl,     -   (mm) (C1-C6 alkyl)NR^(g)SO₂— where R^(g) is H or C1-C6 alkyl,     -   (nn) hetCyc⁵C(═O)NR^(g)— where R^(g) is H or C1-C6 alkyl,     -   (oo) Q-NR^(h)(C1-C3 alkyl)C(═O)NR^(g)— where R^(g) and R^(h) are         independently H or C1-C6 alkyl and Q is H, C1-C6 alkyl or (C1-C6         alkyl)OC(═O)—,     -   (pp)

where R^(g) and R^(h) are independently H or C1-C6 alkyl, Q is H, C1-C6 alkyl or (C1-C6 alkyl)OC(═O)— and r is 1, 2, 3 or 4,

-   -   (qq)

where R^(g) and R^(h) are independently H or C1-C6 alkyl and Q is H, C1-C6 alkyl or (C1-C6 alkyl)OC(═O)—,

-   -   (rr)

where R^(g) is H or C1-C6 alkyl and Q is H, C1-C6 alkyl or (C1-C6 alkyl)OC(═O)—, or

-   -   (ss) R^(g)R^(h)N— where R^(g) and R^(h) are independently H or         C1-C6 alkyl,     -   (tt) (C3-C6 cycloalkyl)C(═O)NR^(g)— where the cycloalkyl is         optionally and independently substituted with one or more         halogens,     -   (uu) (C1-C6 alkyl)C(═O)NR^(g)CH₂— where R^(g) is H or C1-C6         alkyl, or     -   (vv) C1-C6 alkyl)SO₂NR^(g)— where R^(g) is H or C1-C6 alkyl;

Ar¹ is phenyl optionally substituted with one or more substituents independently selected from the group consisting of halogen, CN, C1-C6 alkyl (optionally substituted with 1-3 fluoros), C1-C6 alkoxy (optionally substituted with 1-3 fluoros), (C1-C6 alkoxy)C1-C6 alkyl- (optionally substituted with 1-3 fluoros), C3-C6 cycloalkyl, hydroxyC1-C6 alkyl, (C1-C6 alkyl)SO₂—, R^(e)R^(f)N— and (R^(e)R^(f)N)C1-C6 alkyl- where each R^(e) and R^(f) is independently H or C1-C6 alkyl;

hetAr² is a 5-6 membered heteroaryl ring having 1-3 ring heteroatoms independently selected from N, O and S, or a 9-10 membered bicyclic heteroaryl having 1-2 ring nitrogen atoms, wherein hetAr² is optionally substituted with one or more substituents independently selected from the group consisting of halogen, CN, C1-C6 alkyl (optionally substituted with 1-3 fluoros), C1-C6 alkoxy (optionally substituted with 1-3 fluoros), (C1-C6 alkoxy)C1-C6 alkyl- (optionally substituted with 1-3 fluoros) and hydroxyC1-C6 alkoxy-;

hetCyc⁵ is a 4-6 membered saturated heterocyclic ring having 1-2 ring heteroatoms independently selected from N, O and S wherein said heterocyclic ring is optionally substituted with one or more substituents independently selected from C1-C6 alkoxy and oxo;

R³ is C1-C6 alkyl (optionally substituted with 1-3 fluoros), hydroxyC1-C6 alkyl-, C1-C6 alkoxy, C3-C6 cycloalkyl, (C3-C6 cycloalkyl)CH₂—, (C3-C6 cycloalkyl)O—, (C3-C6 cycloalkyl)CH₂O—, hetCyc⁷O—, Ph-O—, or (C1-C6 alkoxy)C1-C6 alkyl-; wherein each of said C3-C6 cycloalkyl moieties is optionally substituted with C1-C6 alkyl (optionally substituted with 1-3 fluoros), C1-C6 alkoxy, OH or R′R″N— where R′ and R″ are independently hydrogen or C1-C6 alkyl;

R⁴ is H or C1-C6 alkyl;

R⁶ is Ar², hetAr³, Ar²CH₂—, hetCyc⁶-CH₂—, hydroxyC1-C6 alkyl-, (C3-C6 cycloalkyl)CH₂—, or C1-C6 alkyl optionally substituted with 1-3 fluoros;

Ar² is phenyl optionally substituted with one or more substituents independently selected from the group consisting of halogen, CN, C1-C6 alkyl (optionally substituted with 1-3 fluoros), C1-C6 alkoxy (optionally substituted with 1-3 fluoros), (C1-C6 alkoxy)C1-C6 alkyl- (optionally substituted with 1-3 fluoros), C3-C6 cycloalkyl, and R^(g)R^(h)N— where R^(g) and R^(h) are independently H or C1-C6 alkyl, or Ar² is phenyl fused to a 6 membered heterocyclic ring having a ring nitrogen atom and optionally substituted with C1-C6 alkyl;

hetAr³ is a 5-6 membered heteroaryl ring having 1-3 ring heteroatoms independently selected from N, O and S and optionally substituted with one or more substituents independently selected from the group consisting of halogen, CN, C1-C6 alkyl (optionally substituted with 1-3 fluoros), C1-C6 alkoxy (optionally substituted with 1-3 fluoros), and (C1-C6 alkoxy)C1-C6 alkyl- (optionally substituted with 1-3 fluoros);

hetAr⁴ is pyridin-4 (1H)-onyl or pyridin-2 (1H)-onyl optionally substituted with one or more substituents independently selected from C1-C6 alkyl and halogen;

hetCyc⁶ is a 5-7 membered heterocyclic ring having 1-3 ring heteroatoms independently selected from N, O and S; and

hetCyc⁷ is a 5-7 membered heterocyclic ring having 1-3 ring heteroatoms independently selected from N, O and S.

In some embodiments, a RET inhibitor (e.g., a first RET inhibitor or a second RET inhibitor) is a compound of the Formula VII:

or a pharmaceutically acceptable salt or solvate thereof, wherein:

X¹, X², X³ and X⁴ are independently CH or N, wherein zero, one or two of X¹, X², X³ and X⁴ is N;

A is CN;

B is:

-   -   (b) C1-C6 alkyl optionally substituted with 1-3 fluoros,     -   (c) hydroxyC2-C6 alkyl- wherein the alkyl portion is optionally         substituted with a C3-C6 cycloalkylidene ring, or     -   (i) (hetCyc^(a))C1-C3 alkyl-;     -   hetCyc^(a) is a 4-6 membered heterocyclic ring having 1-2 ring         heteroatoms independently selected from N and O and optionally         substituted with one or more substituents independently selected         from OH, C1-C6 alkyl (optionally substituted with 1-3 fluoros),         hydroxyC1-C6 alkyl, halogen, (C1-C6 alkyl)C(═O)—, C1-C6 alkoxy,         oxo, and (C1-C6 alkoxy)C(═O)—;

Ring D is a saturated monocyclic 4-7 membered heterocyclic ring having one ring heteroatom which is nitrogen;

each R^(a) is independently C1-C6 alkyl (optionally substituted with 1-3 fluoros);

R^(b) is (a) hydroxy;

n is 0 or 1;

m is 0 or 1;

E is:

-   -   (e) hetAr²C1-C6 alkyl-,     -   (h) hetAr²—O—,     -   (k) R³C(═O)NR^(g)— where R^(g) is H or C1-C6 alkyl,     -   (l) Ar¹C(═O)NR^(g)— where R^(g) is H or C1-C6 alkyl, or     -   (m) hetAr²C(═O)NR^(g)(CH₂)_(p)— where p is 0 or 1 and R^(g) is H         or C1-C6 alkyl;

Ar¹ is phenyl optionally substituted with one or more substituents independently selected from the group consisting of halogen, CN, C1-C6 alkyl (optionally substituted with 1-3 fluoros), C1-C6 alkoxy (optionally substituted with 1-3 fluoros), (C1-C6 alkoxy)C1-C6 alkyl- (optionally substituted with 1-3 fluoros), C3-C6 cycloalkyl, hydroxyC1-C6 alkyl, (C1-C6 alkyl)SO₂—, R^(e)R^(f)N— and (R^(e)R^(f)N)C1-C6 alkyl- where each R^(e) and R^(f) is independently H or C1-C6 alkyl;

hetAr² is a 5-6 membered heteroaryl ring having 1-3 ring heteroatoms independently selected from N, O and S, or a 9-10 membered bicyclic heteroaryl having 1-2 ring nitrogen atoms, wherein hetAr² is optionally substituted with one or more substituents independently selected from the group consisting of halogen, CN, C1-C6 alkyl (optionally substituted with 1-3 fluoros), C1-C6 alkoxy (optionally substituted with 1-3 fluoros), (C1-C6 alkoxy)C1-C6 alkyl- (optionally substituted with 1-3 fluoros) and hydroxyC1-C6 alkoxy-; and

R³ is C1-C6 alkyl (optionally substituted with 1-3 fluoros), hydroxyC1-C6 alkyl-, C1-C6 alkoxy, C3-C6 cycloalkyl, (C3-C6 cycloalkyl)CH₂—, (C3-C6 cycloalkyl)O—, (C3-C6 cycloalkyl)CH₂O—, hetCyc⁷O—, Ph-O—, or (C1-C6 alkoxy)C1-C6 alkyl-; wherein each of said C3-C6 cycloalkyl moieties is optionally substituted with C1-C6 alkyl (optionally substituted with 1-3 fluoros), C1-C6 alkoxy, OH, or R′R″N— where R′ and R″ are independently hydrogen or C1-C6 alkyl.

In some embodiments, a RET inhibitor which is not a compound of Formula I is selected from the group consisting of: N-(1-(5-(3-cyano-6-(2-hydroxy-2-methylpropoxy)pyrazolo[1,5-a]pyridin-4-yl)pyridin-2-yl)-4-methylpiperidin-4-yl)benzamide; 6-ethoxy-4-(6-(4-hydroxy-4-(pyridin-2-ylmethyl)piperidin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-hydroxy-2-methyl propoxy)-4-(6-(3-(pyridin-2-yloxy)azetidin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-hydroxy-2-methylpropoxy)-4-(6-(4-((6-methoxypyridazin-3-yl)oxy)piperidin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; (S)-6-(2-hydroxy-2-methylpropoxy)-4-(6-(3-(pyridin-2-yloxy)pyrrolidin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; N-(1-(5-(3-cyano-6-((3-fluoro-1-methylazetidin-3-yl)methoxy)pyrazolo[1,5-a]pyridin-4-yl)pyridin-2-yl)-4-methylpiperidin-4-yl)-5-fluoro-2-methylbenzamide; 3-chloro-N-(1-(5-(3-cyano-6-((3-fluoro-1-methylazetidin-3-yl)methoxy)pyrazolo[1,5-a]pyridin-4-yl)pyridin-2-yl)-4-methylpiperidin-4-yl)picolinamide; N-((3S,4S)-1-(5-(3-cyano-6-ethoxypyrazolo[1,5-a]pyridin-4-yl)pyridin-2-yl)-3-hydroxypiperidin-4-yl)-3-methylbutanamide; 6-(2-hydroxy-2-methylpropoxy)-4-(6-(4-hydroxy-4-(pyridin-2-ylmethyl)piperidin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; and 3-chloro-N-((3S,4S)-1-(5-(3-cyano-6-ethoxypyrazolo[1,5-a]pyridin-4-yl)pyrazin-2-yl)-3-hydroxypiperidin-4-yl)picolinamide; or a pharmaceutically acceptable salt or solvate thereof.

Non-limiting examples of receptor tyrosine kinase (e.g., Trk) targeted therapeutic agents, include afatinib, cabozantinib, cetuximab, crizotinib, dabrafenib, entrectinib, erlotinib, gefitinib, imatinib, lapatinib, lestaurtinib, nilotinib, pazopanib, panitumumab, pertuzumab, sunitinib, trastuzumab, 1-((3S,4R)-4-(3-fluorophenyl)-1-(2-methoxyethyl)pyrrolidin-3-yl)-3-(4-methyl-3-(2-methylpyrimidin-5-yl)-I-phenyl-IH-pyrazol-5-yl)urea, AG 879, AR-772, AR-786, AR-256, AR-618, AZ-23, AZ623, DS-6051, Gö 6976, GNF-5837, GTx-186, GW 441756, LOXO-101, MGCD516, PLX7486, RXDX101, VM-902A, TPX-0005, and TSR-011. Additional Trk targeted therapeutic agents include those described in U.S. Pat. Nos. 8,450,322; 8,513,263; 8,933,084; 8,791,123; 8,946,226; 8,450,322; 8,299,057; and 8,912,194; U.S. Publication No. 2016/0137654; 2015/0166564; 2015/0051222; 2015/0283132; and 2015/0306086; International Publication No. WO 2010/033941; WO 2010/048314; WO 2016/077841; WO 2011/146336; WO 2011/006074; WO 2010/033941; WO 2012/158413; WO 2014078454; WO 2014078417; WO 2014078408; WO 2014078378; WO 2014078372; WO 2014078331; WO 2014078328; WO 2014078325; WO 2014078323; WO 2014078322; WO 2015175788; WO 2009/013126; WO 2013/174876; WO 2015/124697; WO 2010/058006; WO 2015/017533; WO 2015/112806; WO 2013/183578; and WO 2013/074518, all of which are hereby incorporated by reference in their entireties.

Further examples of Trk inhibitors can be found in U.S. Pat. No. 8,637,516, International Publication No. WO 2012/034091, U.S. Pat. No. 9,102,671, International Publication No. WO 2012/116217, U.S. Publication No. 2010/0297115, International Publication No. WO 2009/053442, U.S. Pat. No. 8,642,035, International Publication No. WO 2009092049, U.S. Pat. No. 8,691,221, International Publication No. WO2006131952, all of which are incorporated by reference in their entireties herein. Exemplary Trk inhibitors include GNF-4256, described in Cancer Chemother. Pharmacol. 75(1):131-141, 2015; and GNF-5837 (N-[3-[[2,3-dihydro-2-oxo-3-(1H-pyrrol-2-ylmethylene)-1H-indol-6-yl]amino]-4-methylphenyl]-N′-[2-fluoro-5-(trifluoromethyl)phenyl]-urea), described in ACS Med. Chem. Lett. 3(2):140-145, 2012, each of which is incorporated by reference in its entirety herein.

Additional examples of Trk inhibitors include those disclosed in U.S. Publication No. 2010/0152219, U.S. Pat. No. 8,114,989, and International Publication No. WO 2006/123113, all of which are incorporated by reference in their entireties herein. Exemplary Trk inhibitors include AZ623, described in Cancer 117(6):1321-1391, 2011; AZD6918, described in Cancer Biol. Ther. 16(3):477-483, 2015; AZ64, described in Cancer Chemother. Pharmacol. 70:477-486, 2012; AZ-23 ((S)-5-Chloro-N2-(1-(5-fluoropyridin-2-yl)ethyl)-N4-(5-isopropoxy-1H-pyrazol-3-yl)pyrimidine-2,4-diamine), described in Mol. Cancer Ther. 8:1818-1827, 2009; and AZD7451; each of which is incorporated by reference in its entirety.

A Trk inhibitor can include those described in U.S. Pat. Nos. 7,615,383; 7,384,632; 6,153,189; 6,027,927; 6,025,166; 5,910,574; 5,877,016; and 5,844,092, each of which is incorporated by reference in its entirety.

Further examples of Trk inhibitors include CEP-751, described in Int. J. Cancer 72:672-679, 1997; CT327, described in Acta Derm. Venereol. 95:542-548, 2015; compounds described in International Publication No. WO 2012/034095; compounds described in U.S. Pat. No. 8,673,347 and International Publication No. WO 2007/022999; compounds described in U.S. Pat. No. 8,338,417; compounds described in International Publication No. WO 2016/027754; compounds described in U.S. Pat. No. 9,242,977; compounds described in U.S. Publication No. 2016/0000783; sunitinib (N-(2-diethylaminoethyl)-5-[(Z)-(5-fluoro-2-oxo-1H-indol-3-ylidene)methyl]-2,4-dimethyl-1H-pyrrole-3-carboxamide), as described in PLoS One 9:e95628, 2014; compounds described in International Publication No. WO 2011/133637; compounds described in U.S. Pat. No. 8,637,256; compounds described in Expert. Opin. Ther. Pat. 24(7):731-744, 2014; compounds described in Expert Opin. Ther. Pat. 19(3):305-319, 2009; (R)-2-phenylpyrrolidine substituted imidazopyridazines, e.g., GNF-8625, (R)-1-(6-(6-(2-(3-fluorophenyl)pyrrolidin-1-yl)imidazo[1,2-b]pyridazin-3-yl)-[2,4′-bipyridin]-2′-yl)piperidin-4-ol as described in ACS Med. Chem. Lett. 6(5):562-567, 2015; GTx-186 and others, as described in PLoS One 8(12):e83380, 2013; K252a ((9S-(9α,10β,12α))-2,3,9,10,11,12-hexahydro-10-hydroxy-10-(methoxycarbonyl)-9-methyl-9,12-epoxy-1H-diindolo[1,2,3-fg:3′,2′,1′-kl]pyrrolo[3,4-i][1,6]benzodiazocin-1-one), as described in Mol. Cell Biochem. 339 (1-2):201-213, 2010; 4-aminopyrazolylpyrimidines, e.g., AZ-23 (((S)-5-chloro-N2-(1-(5-fluoropyridin-2-yl)ethyl)-N4-(5-isopropoxy-1H-pyrazol-3-yl)pyrimidine-2,4-diamine)), as described in J. Med. Chem. 51(15):4672-4684, 2008; PHA-739358 (danusertib), as described in Mol. Cancer Ther. 6:3158, 2007; Go 6976 (5,6,7,13-tetrahydro-13-methyl-5-oxo-12H-indolo[2,3-a]pyrrolo[3,4-c]carbazole-12-propanenitrile), as described in J. Neurochem. 72:919-924, 1999; GW441756 ((3Z)-3-[(1-methylindol-3-yl)methylidene]-1H-pyrrolo[3,2-b]pyridin-2-one), as described in JAE 115:117, 2010; milciclib (PHA-848125AC), described in J. Carcinog. 12:22, 2013; AG-879 ((2E)-3-[3,5-Bis(1,1-dimethylethyl)-4-hydroxyphenyl]-2-cyano-2-propenethioamide); altiratinib (N-(4-((2-(cyclopropanecarboxamido)pyridin-4-yl)oxy)-2,5-difluorophenyl)-N-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide); cabozantinib (N-(4-((6,7-Dimethoxyquinolin-4-yl)oxy)phenyl)-N′-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide); lestaurtinib ((5S,6S,8R)-6-Hydroxy-6-(hydroxymethyl)-5-methyl-7,8,14,15-tetrahydro-5H-16-oxa-4b,8a,14-triaza-5,8-methanodibenzo[b,h]cycloocta[jkl]cyclopenta[e]-as-indacen-13 (6H)-one); dovatinib (4-amino-5-fluoro-3-[6-(4-methylpiperazin-1-yl)-1H-benzimidazol-2-yl]quinolin-2 (1H)-one mono 2-hydroxypropanoate hydrate); sitravatinib (N-(3-fluoro-4-((2-(5-(((2-methoxyethyl)amino)methyl)pyridin-2-yl)thieno[3,2-b]pyridin-7-yl)oxy)phenyl)-N-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide); ONO-5390556; regorafenib (4-[4-({[4-Chloro-3-(trifluoromethyl)phenyl]carbamoyl}amino)-3-fluorophenoxy]-N-methylpyridine-2-carboxamide hydrate); and VSR-902A; all of the references above are incorporated by reference in their entireties herein.

The ability of a Trk inhibitor to act as a TrkA, TrkB, and/or Trk C inhibitor may be tested using the assays described in Examples A and B in U.S. Pat. No. 8,513,263, which is incorporated herein by reference.

In some embodiments, signal transduction pathway inhibitors include Ras-Raf-MEK-ERK pathway inhibitors (e.g., binimetinib, selumetinib, encorafinib, sorafenib, trametinib, and vemurafenib), PI3K-Akt-mTOR-S6K pathway inhibitors (e.g. everolimus, rapamycin, perifosine, temsirolimus), and other kinase inhibitors, such as baricitinib, brigatinib, capmatinib, danusertib, ibrutinib, milciclib, quercetin, regorafenib, ruxolitinib, semaxanib, AP32788, BLU285, BLU554, INCB39110, INCB40093, INCB50465, INCB52793, INCB54828, MGCD265, NMS-088, NMS-1286937, PF 477736 ((R)-amino-N-[5,6-dihydro-2-(1-methyl-1H-pyrazol-4-yl)-6-oxo-1Hpyrrolo[4,3,2-ef][2,3]benzodiazepin-8-yl]-cyclohexaneacetamide), PLX3397, PLX7486, PLX8394, PLX9486, PRN1008, PRN1371, RXDX103, RXDX106, RXDX108, and TG101209 (N-tert-butyl-3-(5-methyl-2-(4-(4-methylpiperazin-1-yl)phenylamino)pyrimidin-4-ylamino)benzenesulfonamide).

Non-limiting examples of checkpoint inhibitors include ipilimumab, tremelimumab, nivolumab, pidilizumab, MPDL3208A, MED14736, MSB0010718C, BMS-936559, BMS-956559, BMS-935559 (MDX-1105), AMP-224, and pembrolizumab.

In some embodiments, cytotoxic chemotherapeutics are selected from arsenic trioxide, bleomycin, cabazitaxel, capecitabine, carboplatin, cisplatin, cyclophosphamide, cytarabine, dacarbazine, daunorubicin, docetaxel, doxorubicin, etoposide, fluorouracil, gemcitabine, irinotecan, lomustine, methotrexate, mitomycin C, oxaliplatin, paclitaxel, pemetrexed, temozolomide, and vincristine.

Non-limiting examples of angiogenesis-targeted therapies include aflibercept and bevacizumab.

The term “immunotherapy” refers to an agent that modulates the immune system. In some embodiments, an immunotherapy can increase the expression and/or activity of a regulator of the immune system. In some embodiments, an immunotherapy can decrease the expression and/or activity of a regulator of the immune system. In some embodiments, an immunotherapy can recruit and/or enhance the activity of an immune cell.

In some embodiments, the immunotherapy is a cellular immunotherapy (e.g., adoptive T-cell therapy, dendritic cell therapy, natural killer cell therapy). In some embodiments, the cellular immunotherapy is sipuleucel-T (APC8015; Provenge™; Plosker (2011) Drugs 71(1): 101-108). In some embodiments, the cellular immunotherapy includes cells that express a chimeric antigen receptor (CAR). In some embodiments, the cellular immunotherapy is a CAR-T cell therapy. In some embodiments, the CAR-T cell therapy is tisagenlecleucel (Kymriah™).

In some embodiments, the immunotherapy is an antibody therapy (e.g., a monoclonal antibody, a conjugated antibody). In some embodiments, the antibody therapy is bevacizumab (Mvasti™, Avastin®), trastuzumab (Herceptin®), avelumab (Bavencio®), rituximab (MabThera™, Rituxan®), edrecolomab (Panorex), daratumuab (Darzalex®), olaratumab (Lartruvo™), ofatumumab (Arzerra®), alemtuzumab (Campath®), cetuximab (Erbitux®), oregovomab, pembrolizumab (Keytruda®), dinutiximab (Unituxin®), obinutuzumab (Gazyva®), tremelimumab (CP-675,206), ramucirumab (Cyramza®), ublituximab (TG-1101), panitumumab (Vectibix®), elotuzumab (Empliciti™), avelumab (Bavencio®), necitumumab (Portrazza™), cirmtuzumab (UC-961), ibritumomab (Zevalin®), isatuximab (SAR650984), nimotuzumab, fresolimumab (GC1008), lirilumab (INN), mogamulizumab (Poteligeo®), ficlatuzumab (AV-299), denosumab (Xgeva®), ganitumab, urelumab, pidilizumab or amatuximab.

In some embodiments, the immunotherapy is an antibody-drug conjugate. In some embodiments, the antibody-drug conjugate is gemtuzumab ozogamicin (Mylotarg™), inotuzumab ozogamicin (Besponsa®), brentuximab vedotin (Adcetris®), ado-trastuzumab emtansine (TDM-1; Kadcyla®), mirvetuximab soravtansine (IMGN853) or anetumab ravtansine

In some embodiments, the immunotherapy includes blinatumomab (AMG103; Blincyto®) or midostaurin (Rydapt).

In some embodiments, the immunotherapy includes a toxin. In some embodiments, the immunotherapy is denileukin diftitox (Ontak®).

In some embodiments, the immunotherapy is a cytokine therapy. In some embodiments, the cytokine therapy is an interleukin 2 (IL-2) therapy, an interferon alpha (IFNα) therapy, a granulocyte colony stimulating factor (G-CSF) therapy, an interleukin 12 (IL-12) therapy, an interleukin 15 (IL-15) therapy, an interleukin 7 (IL-7) therapy or an erythropoietin-alpha (EPO) therapy. In some embodiments, the IL-2 therapy is aldesleukin (Proleukin®). In some embodiments, the IFNα therapy is IntronA® (Roferon-A®). In some embodiments, the G-CSF therapy is filgrastim (Neupogen®).

In some embodiments, the immunotherapy is an immune checkpoint inhibitor. In some embodiments, the immunotherapy includes one or more immune checkpoint inhibitors. In some embodiments, the immune checkpoint inhibitor is a CTLA-4 inhibitor, a PD-1 inhibitor or a PD-L₁ inhibitor. In some embodiments, the CTLA-4 inhibitor is ipilimumab (Yervoy®) or tremelimumab (CP-675,206). In some embodiments, the PD-1 inhibitor is pembrolizumab (Keytruda®) or nivolumab (Opdivo®). In some embodiments, the PD-L₁ inhibitor is atezolizumab (Tecentriq®), avelumab (Bavencio®) or durvalumab (Imfinzi™).

In some embodiments, the immunotherapy is mRNA-based immunotherapy. In some embodiments, the mRNA-based immunotherapy is CV9104 (see, e.g., Rausch et al. (2014) Human Vaccin Immunother 10(11): 3146-52; and Kubler et al. (2015) J. Immunother Cancer 3:26).

In some embodiments, the immunotherapy is bacillus Calmette-Guerin (BCG) therapy.

In some embodiments, the immunotherapy is an oncolytic virus therapy. In some embodiments, the oncolytic virus therapy is talimogene alherparepvec (T-VEC; Imlygic®).

In some embodiments, the immunotherapy is a cancer vaccine. In some embodiments, the cancer vaccine is a human papillomavirus (HPV) vaccine. In some embodiments, the HPV vaccine is Gardasil®, Gardasil9® or Cervarix®. In some embodiments, the cancer vaccine is a hepatitis B virus (HBV) vaccine. In some embodiments, the HBV vaccine is Engerix-B®, Recombivax HB® or GI-13020 (Tarmogen®). In some embodiments, the cancer vaccine is Twinrix® or Pediarix®. In some embodiments, the cancer vaccine is BiovaxID®, Oncophage®, GVAX, ADXS11-001, ALVAC-CEA, PROSTVAC®, Rindopepimut®, CimaVax-EGF, lapuleucel-T (APC8024; Neuvenge™), GRNVAC1, GRNVAC2, GRN-1201, hepcortespenlisimut-L (Hepko-V5), DCVAX®, SCIB1, BMT CTN 1401, PrCa VBIR, PANVAC, ProstAtak®, DPX-Survivac, or viagenpumatucel-L (HS-110).

In some embodiments, the immunotherapy is a peptide vaccine. In some embodiments, the peptide vaccine is nelipepimut-S (E75) (NeuVax™), IMA901, or SurVaxM (SVN53-67). In some embodiments, the cancer vaccine is an immunogenic personal neoantigen vaccine (see, e.g., Ott et al. (2017) Nature 547: 217-221; Sahin et al. (2017) Nature 547: 222-226). In some embodiments, the cancer vaccine is RGSH4K, or NEO-PV-01. In some embodiments, the cancer vaccine is a DNA-based vaccine. In some embodiments, the DNA-based vaccine is a mammaglobin-A DNA vaccine (see, e.g., Kim et al. (2016) Oncolmmunology 5 (2): e1069940).

In some embodiments, immune-targeted agents are selected from aldesleukin, interferon alfa-2b, ipilimumab, lambrolizumab, nivolumab, prednisone, and sipuleucel-T.

Non-limiting examples of radiotherapy include radioiodide therapy, external-beam radiation, and radium 223 therapy.

Additional kinase inhibitors include those described in, for example, U.S. Pat. Nos. 7,514,446; 7,863,289; 8,026,247; 8,501,756; 8,552,002; 8,815,901; 8,912,204; 9,260,437; 9,273,051; U.S. Publication No. US 2015/0018336; International Publication No. WO 2007/002325; WO 2007/002433; WO 2008/080001; WO 2008/079906; WO 2008/079903; WO 2008/079909; WO 2008/080015; WO 2009/007748; WO 2009/012283; WO 2009/143018; WO 2009/143024; WO 2009/014637; 2009/152083; WO 2010/111527; WO 2012/109075; WO 2014/194127; WO 2015/112806; WO 2007/110344; WO 2009/071480; WO 2009/118411; WO 2010/031816; WO 2010/145998; WO 2011/092120; WO 2012/101032; WO 2012/139930; WO 2012/143248; WO 2012/152763; WO 2013/014039; WO 2013/102059; WO 2013/050448; WO 2013/050446; WO 2014/019908; WO 2014/072220; WO 2014/184069; and WO 2016/075224 all of which are hereby incorporated by reference in their entireties.

Further examples of kinase inhibitors include those described in, for example, WO 2016/081450; WO 2016/022569; WO 2016/011141; WO 2016/011144; WO 2016/011147; WO 2015/191667; WO 2012/101029; WO 2012/113774; WO 2015/191666; WO 2015/161277; WO 2015/161274; WO 2015/108992; WO 2015/061572; WO 2015/058129; WO 2015/057873; WO 2015/017528; WO/2015/017533; WO 2014/160521; and WO 2014/011900, each of which is hereby incorporated by reference in its entirety.

Further examples of kinase inhibitors include luminespib (AUY-922, NVP-AUY922) (5-(2,4-dihydroxy-5-isopropylphenyl)-N-ethyl-4-(4-(morpholinomethyl)phenyl)isoxazole-3-carboxamide) and doramapimod (BIRB-796) (1-[5-tert-butyl-2-(4-methylphenyl)pyrazol-3-yl]-3-[4-(2-morpholin-4-ylethoxy)naphthalen-1-yl]urea).

Accordingly, also provided herein is a method of treating cancer, comprising administering to a patient in need thereof a pharmaceutical combination for treating cancer which comprises (a) a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof, (b) an additional therapeutic agent, and (c) optionally at least one pharmaceutically acceptable carrier for simultaneous, separate or sequential use for the treatment of cancer, wherein the amounts of the compound of Formula I or a pharmaceutically acceptable salt or solvate thereof and the additional therapeutic agent are together effective in treating the cancer.

In some embodiments, the additional therapeutic agent(s) includes any one of the above listed therapies or therapeutic agents which are standards of care in cancers wherein the cancer has a dysregulation of a RET gene, a RET protein, or expression or activity, or level of any of the same.

These additional therapeutic agents may be administered with one or more doses of the compound of Formula I, or a pharmaceutically acceptable salt or solvate thereof, or pharmaceutical composition thereof, as part of the same or separate dosage forms, via the same or different routes of administration, and/or on the same or different administration schedules according to standard pharmaceutical practice known to one skilled in the art.

Also provided herein is (i) a pharmaceutical combination for treating a cancer in a patient in need thereof, which comprises (a) a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof, (b) at least one additional therapeutic agent (e.g., any of the exemplary additional therapeutic agents described herein or known in the art), and (c) optionally at least one pharmaceutically acceptable carrier for simultaneous, separate or sequential use for the treatment of cancer, wherein the amounts of the compound of Formula I or pharmaceutically acceptable salt or solvate thereof and of the additional therapeutic agent are together effective in treating the cancer; (ii) a pharmaceutical composition comprising such a combination; (iii) the use of such a combination for the preparation of a medicament for the treatment of cancer; and (iv) a commercial package or product comprising such a combination as a combined preparation for simultaneous, separate or sequential use; and to a method of treatment of cancer in a patient in need thereof. In one embodiment the patient is a human. In some embodiments, the cancer is a RET-associated cancer. For example, a RET-associated cancer having one or more RET inhibitor resistance mutations.

The term “pharmaceutical combination”, as used herein, refers to a pharmaceutical therapy resulting from the mixing or combining of more than one active ingredient and includes both fixed and non-fixed combinations of the active ingredients. The term “fixed combination” means that a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof and at least one additional therapeutic agent (e.g., a chemotherapeutic agent), are both administered to a patient simultaneously in the form of a single composition or dosage. The term “non-fixed combination” means that a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof and at least one additional therapeutic agent (e.g., chemotherapeutic agent) are formulated as separate compositions or dosages such that they may be administered to a patient in need thereof simultaneously, concurrently or sequentially with variable intervening time limits, wherein such administration provides effective levels of the two or more compounds in the body of the patient. These also apply to cocktail therapies, e.g. the administration of three or more active ingredients

Accordingly, also provided herein is a method of treating a cancer, comprising administering to a patient in need thereof a pharmaceutical combination for treating cancer which comprises (a) a compound of Formula I or pharmaceutically acceptable salt or solvate thereof, (b) an additional therapeutic agent, and (c) optionally at least one pharmaceutically acceptable carrier for simultaneous, separate or sequential use for the treatment of cancer, wherein the amounts of the compound of Formula I or pharmaceutically acceptable salt or solvate thereof and the additional therapeutic agent are together effective in treating the cancer. In one embodiment, the compound of Formula I or pharmaceutically acceptable salt or solvate thereof, and the additional therapeutic agent are administered simultaneously as separate dosages. In one embodiment, the compound of Formula I or pharmaceutically acceptable salt or solvate thereof, and the additional therapeutic agent are administered as separate dosages sequentially in any order, in jointly therapeutically effective amounts, e.g. in daily or intermittently dosages. In one embodiment, the compound of Formula I or pharmaceutically acceptable salt or solvate thereof, and the additional therapeutic agent are administered simultaneously as a combined dosage. In some embodiments, the cancer is a RET-associated cancer. For example, a RET-associated cancer having one or more RET inhibitor resistance mutations.

Also provided herein is a method of treating a disease or disorder mediated by RET in a patient in need of such treatment, the method comprising administering to the patient a therapeutically effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof or a pharmaceutical composition thereof. In some embodiments, the disease or disorder mediated by RET is a dysregulation of RET gene, a RET kinase, or expression or activity or level of any of the same. For example the dysregulation of a RET gene, a RET kinase, or expression or activity or level of any of the same includes one or more RET inhibitor resistance mutations. A disease or disorder mediated by RET can include any disease, disorder or condition that is directly or indirectly linked to expression or activity of RET, including overexpression and/or abnormal activity levels. In one embodiment, the disease is cancer (e.g., a RET-associated cancer). In one embodiment, the cancer is any of the cancers or RET-associated cancers described herein.

Although the genetic basis of tumorigenesis may vary between different cancer types, the cellular and molecular mechanisms required for metastasis appear to be similar for all solid tumor types. During a metastatic cascade, the cancer cells lose growth inhibitory responses, undergo alterations in adhesiveness and produce enzymes that can degrade extracellular matrix components. This leads to detachment of tumor cells from the original tumor, infiltration into the circulation through newly formed vasculature, migration and extravasation of the tumor cells at favorable distant sites where they may form colonies. A number of genes have been identified as being promoters or suppressors of metastasis. For example, overexpression of glial cell-derived neurotrophic factor (GDNF) and its RET receptor tyrosine kinase have been correlated with cancer proliferation and metastasis. See, e.g., Zeng, Q. et al. J. Int. Med. Res. (2008) 36(4): 656-64.

Accordingly, also provided herein are methods for inhibiting, preventing, aiding in the prevention, or decreasing the symptoms of metastasis of a cancer in a patient in need thereof, the method comprising administering to the patient a therapeutically effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof or a pharmaceutical composition thereof. Such methods can be used in the treatment of one or more of the cancers described herein. See, e.g., US Publication No. 2013/0029925; International Publication No. WO 2014/083567; and U.S. Pat. No. 8,568,998. See also, e.g., Hezam K et al., Rev Neurosci 2018 Jan. 26; 29:93-98; Gao L, et al., Pancreas 2015 January; 44:134-143; Ding K et al., J Biol Chem 2014 Jun. 6; 289:16057-71; and Amit M et al., Oncogene 2017 Jun. 8; 36:3232-3239. In some embodiments, the cancer is a RET-associated cancer. In some embodiments, the compound of Formula I or a pharmaceutically acceptable salt or solvate thereof is used in combination with an additional therapy or another therapeutic agent, including a chemotherapeutic agent, such as a kinase inhibitor. For example, a first or second RET kinase inhibitor.

The term “metastasis” is an art known term and means the formation of an additional tumor (e.g., a solid tumor) at a site distant from a primary tumor in a subject or patient, where the additional tumor includes the same or similar cancer cells as the primary tumor.

Also provided are methods of decreasing the risk of developing a metastasis or an additional metastasis in a patient having a RET-associated cancer that include: selecting, identifying, or diagnosing a patient as having a RET-associated cancer, and administering a therapeutically effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof to the patient selected, identified, or diagnosed as having a RET-associated cancer. Also provided are methods of decreasing the risk of developing a metastasis or an additional metastasis in a patient having a RET-associated cancer that includes administering a therapeutically effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvent thereof to a patient having a RET-associated cancer. The decrease in the risk of developing a metastasis or an additional metastasis in a patient having a RET-associated cancer can be compared to the risk of developing a metastasis or an additional metastasis in the patient prior to treatment, or as compared to a patient or a population of patients having a similar or the same RET-associated cancer that has received no treatment or a different treatment. In some embodiments, the RET-associated cancer is a RET-associated cancer having one or more RET inhibitor resistance mutations.

The phrase “risk of developing a metastasis” means the risk that a subject or patient having a primary tumor will develop an additional tumor (e.g., a solid tumor) at a site distant from a primary tumor in a subject or patient over a set period of time, where the additional tumor includes the same or similar cancer cells as the primary tumor. Methods for reducing the risk of developing a metastasis in a subject or patient having a cancer are described herein.

The phrase “risk of developing additional metastases” means the risk that a subject or patient having a primary tumor and one or more additional tumors at sites distant from the primary tumor (where the one or more additional tumors include the same or similar cancer cells as the primary tumor) will develop one or more further tumors distant from the primary tumor, where the further tumors include the same or similar cancer cells as the primary tumor. Methods for reducing the risk of developing additional metastasis are described herein.

In some embodiments, the presence of one or more RET inhibitor resistance mutations in a tumor causes the tumor to be more resistant to treatment with a first RET inhibitor. Methods useful when a RET inhibitor resistance mutation causes the tumor to be more resistant to treatment with a first RET inhibitor are described below. For example, provided herein are methods of treating a subject having a cancer that include: identifying a subject having a cancer cell that has one or more RET inhibitor resistance mutations; and administering to the identified subject a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the compound of Formula I or a pharmaceutically acceptable salt or solvate thereof is administered in combination with the first RET inhibitor. Also provided are methods of treating a subject identified as having a cancer cell that has one or more RET inhibitor resistance mutations that include administering to the subject a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the compound of Formula I or a pharmaceutically acceptable salt or solvate thereof is administered in combination with the first RET inhibitor. In some embodiments, the one or more RET inhibitor resistance mutations confer increased resistance to a cancer cell or tumor to treatment with the first RET inhibitor. In some embodiments, the one or more RET inhibitor resistance mutations include one or more RET inhibitor resistance mutations listed in Tables 3 and 4. For example, the one or more RET inhibitor resistance mutations can include a substitution at amino acid position 804, e.g., V804M, V804L, or V804E.

For example, provided herein are methods for treating a RET-associated cancer in a subject in need of such treatment, the method comprising (a) detecting a dysregulation of a RET gene, a RET kinase, or the expression or activity or level of any of the same in a sample from the subject; and (b) administering to the subject a therapeutically effective amount of a first RET inhibitor, wherein the first RET inhibitor is selected from the group consisting of alectinib, cabozantinib, lenvatinib, nintedanib, ponatinib, regorfenib, sorafenib, sunitinib, vandetanib, RXDX-105 (agerafenib), LOXO-292, BLU-667, BLU6864, DS-5010, GSK3179106, GSK3352589, and NMS-E668. In some embodiments, the methods further comprise (after (b)) (c) determining whether a cancer cell in a sample obtained from the subject has at least one RET inhibitor resistance mutation; and (d) administering a compound of Formula I, or a pharmaceutically acceptable salt or solvate thereof as a monotherapy or in conjunction with another anticancer agent to the subject if the subject has a cancer cell that has at least one RET inhibitor resistance mutation; or (e) administering additional doses of the first RET inhibitor of step (b) to the subject if the subject has a cancer cell that does not have a RET inhibitor resistance mutation.

In some embodiments, provided herein are methods for treating a RET-associated cancer in a subject in need of such treatment, the method comprising (a) detecting a dysregulation of a RET gene, a RET kinase, or the expression or activity or level of any of the same in a sample from the subject; and (b) administering to the subject a therapeutically effective amount of a first RET inhibitor, wherein the first RET inhibitor is selected from the group consisting of alectinib, cabozantinib, lenvatinib, nintedanib, ponatinib, regorfenib, sorafenib, sunitinib, vandetanib, RXDX-105 (agerafenib), LOXO-292, BLU-667, BLU6864, DS-5010, GSK3179106, GSK3352589, and NMS-E668. In some embodiments, the methods further comprise (after (b)) (c) determining whether a cancer cell in a sample obtained from the subject has at least one RET inhibitor resistance mutation; and (d) administering a compound of Formula I selected from i) Example No. 1-20; ii) Example No. 21-40; iii) Example No. 41-49; iv) Example No. 50-70; v) Example No. 71-90; vi) Example No. 91-110; vii) Example No. 111-121, or a pharmaceutically acceptable salt or solvate thereof as a monotherapy or in conjunction with another anticancer agent to the subject if the subject has a cancer cell that has at least one RET inhibitor resistance mutation; or (e) administering additional doses of the first RET inhibitor of step (b) to the subject if the subject has a cancer cell that does not have a RET inhibitor resistance mutation.

In some embodiments, provided herein are methods for treating a RET-associated cancer in a subject in need of such treatment, the method comprising (a) detecting one or more fusion proteins of Table 1 and/or one or more RET kinase protein point mutations/insertions/deletions of Tables 2 and 2a in a sample from the subject; and (b) administering to the subject a therapeutically effective amount of a first RET inhibitor, wherein the first RET inhibitor is selected from the group consisting of alectinib, cabozantinib, lenvatinib, nintedanib, ponatinib, regorfenib, sorafenib, sunitinib, vandetanib, RXDX-105 (agerafenib), LOXO-292, BLU-667, BLU6864, DS-5010, GSK3179106, GSK3352589, and NMS-E668. In some embodiments, the methods further comprise (after (b)) (c) determining whether a cancer cell in a sample obtained from the subject has at least one RET inhibitor resistance mutation of Tables 3 or 4; and (d) administering a compound of Formula I selected from i) Example No. 1-20; ii) Example No. 21-40; iii) Example No. 41-49; iv) Example No. 50-70; v) Example No. 71-90; vi) Example No. 91-110; vii) Example No. 111-121, or a pharmaceutically acceptable salt or solvate thereof as a monotherapy or in conjunction with another anticancer agent to the subject if the subject has a cancer cell that has at least one RET inhibitor resistance mutation; or (e) administering additional doses of the first RET inhibitor of step (b) to the subject if the subject has a cancer cell that does not have a RET inhibitor resistance mutation.

In some embodiments, provided herein are methods for treating a RET-associated cancer in a subject in need of such treatment, the method comprising (a) detecting the fusion protein KIF5B-RET in a sample from the subject; and (b) administering to the subject a therapeutically effective amount of a first RET inhibitor, wherein the first RET inhibitor is selected from the group consisting of alectinib, cabozantinib, lenvatinib, nintedanib, ponatinib, regorfenib, sorafenib, sunitinib, vandetanib, RXDX-105 (agerafenib), LOXO-292, BLU-667, BLU6864, DS-5010, GSK3179106, GSK3352589, and NMS-E668. In some embodiments, the methods further comprise (after (b)) (c) determining whether a cancer cell in a sample obtained from the subject has the RET inhibitor resistance mutation V804M; and (d) administering a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof selected from the group consisting of a compound of Formula I selected from i) Example No. 1-20; ii) Example No. 21-40; iii) Example No. 41-49; iv) Example No. 50-70; v) Example No. 71-90; vi) Example No. 91-110; vii) Example No. 111-121, or a pharmaceutically acceptable salt or solvate thereof as a monotherapy or in conjunction with another anticancer agent to the subject if the subject has a cancer cell that has at least one RET inhibitor resistance mutation; or (e) administering additional doses of the first RET inhibitor of step (b) to the subject if the subject has a cancer cell that does not have a RET inhibitor resistance mutation.

As another example, provided herein are methods for treating a RET-associated cancer in a subject in need of such treatment, the method comprising (a) detecting a dysregulation of a RET gene, a RET kinase, or the expression or activity or level of any of the same in a sample from the subject; and (b) administering to the subject a therapeutically effective amount of a compound of Formula I, or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the methods further comprise (after (b)) (c) determining whether a cancer cell in a sample obtained from the subject has at least one RET inhibitor resistance mutation; and (d) administering a second RET inhibitor, wherein the second RET inhibitor is selected from the group consisting of alectinib, cabozantinib, lenvatinib, nintedanib, ponatinib, regorfenib, sorafenib, sunitinib, vandetanib, RXDX-105 (agerafenib), LOXO-292, BLU-667, BLU6864, DS-5010, GSK3179106, GSK3352589, and NMS-E668, as a monotherapy or in conjunction with another anticancer agent to the subject if the subject has a cancer cell that has at least one RET inhibitor resistance mutation; or (e) administering additional doses of the compound of Formula I or a pharmaceutically acceptable salt or solvate thereof of step (b) to the subject if the subject has a cancer cell that does not have a RET inhibitor resistance mutation. In some embodiments, provided herein are methods for treating a RET-associated cancer in a subject in need of such treatment, the method comprising (a) detecting a dysregulation of a RET gene, a RET kinase, or the expression or activity or level of any of the same in a sample from the subject; and (b) administering to the subject a therapeutically effective amount of a compound of Formula I selected from i) Example No. 1-20; ii) Example No. 21-40; iii) Example No. 41-49; iv) Example No. 50-70; v) Example No. 71-90; vi) Example No. 91-110; vii) Example No. 111-121, or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the methods further comprise (after (b)) (c) determining whether a cancer cell in a sample obtained from the subject has at least one RET inhibitor resistance mutation; and (d) administering a second RET inhibitor, wherein the second RET inhibitor is selected from the group consisting of alectinib, cabozantinib, lenvatinib, nintedanib, ponatinib, regorfenib, sorafenib, sunitinib, vandetanib, RXDX-105 (agerafenib), LOXO-292, BLU-667, BLU6864, DS-5010, GSK3179106, GSK3352589, and NMS-E668, as a monotherapy or in conjunction with another anticancer agent to the subject if the subject has a cancer cell that has at least one RET inhibitor resistance mutation; or (e) administering additional doses of the compound of Formula I or a pharmaceutically acceptable salt or solvate thereof of step (b) to the subject if the subject has a cancer cell that does not have a RET inhibitor resistance mutation. In some embodiments, provided herein are methods for treating a RET-associated cancer in a subject in need of such treatment, the method comprising (a) detecting one or more fusion proteins of Table 1 and/or one or more RET kinase protein point mutations/insertions/deletions of Tables 2 and 2a in a sample from the subject; and (b) administering to the subject a therapeutically effective amount of a compound of Formula I selected from i) Example No. 1-20; ii) Example No. 21-40; iii) Example No. 41-49; iv) Example No. 50-70; v) Example No. 71-90; vi) Example No. 91-110; vii) Example No. 111-121, or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the methods further comprise (after (b)) (c) determining whether a cancer cell in a sample obtained from the subject has at least one RET inhibitor resistance mutation of Tables 3 or 4; and (d) administering a second RET inhibitor, wherein the second RET inhibitor is selected from the group consisting of alectinib, cabozantinib, lenvatinib, nintedanib, ponatinib, regorfenib, sorafenib, sunitinib, vandetanib, RXDX-105 (agerafenib), LOXO-292, BLU-667, BLU6864, DS-5010, GSK3179106, GSK3352589, and NMS-E668, as a monotherapy or in conjunction with another anticancer agent to the subject if the subject has a cancer cell that has at least one RET inhibitor resistance mutation; or (e) administering additional doses of the compound of Formula I or a pharmaceutically acceptable salt or solvate thereof of step (b) to the subject if the subject has a cancer cell that does not have a RET inhibitor resistance mutation. In some embodiments, provided herein are methods for treating a RET-associated cancer in a subject in need of such treatment, the method comprising (a) detecting the fusion protein KIF5B-RET in a sample from the subject; and (b) administering to the subject a therapeutically effective amount of a compound of Formula I selected from i) Example No. 1-20; ii) Example No. 21-40; iii) Example No. 41-49; iv) Example No. 50-70; v) Example No. 71-90; vi) Example No. 91-110; vii) Example No. 111-121, or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the methods further comprise (after (b)) (c) determining whether a cancer cell in a sample obtained from the subject has the RET inhibitor resistance mutation V804M; and (d) administering a second RET inhibitor, wherein the second RET inhibitor is selected from the group consisting of alectinib, cabozantinib, lenvatinib, nintedanib, ponatinib, regorfenib, sorafenib, sunitinib, vandetanib, RXDX-105 (agerafenib), LOXO-292, BLU-667, BLU6864, DS-5010, GSK3179106, GSK3352589, and NMS-E668, as a monotherapy or in conjunction with another anticancer agent to the subject if the subject has a cancer cell that has at least one RET inhibitor resistance mutation; or (e) administering additional doses of the compound of Formula I or a pharmaceutically acceptable salt or solvate thereof of step (b) to the subject if the subject has a cancer cell that does not have a RET inhibitor resistance mutation.

In some embodiments, the presence of one or more RET inhibitor resistance mutations in a tumor causes the tumor to be more resistant to treatment with a first RET inhibitor. Methods useful when a RET inhibitor resistance mutation causes the tumor to be more resistant to treatment with a first RET inhibitor are described below. For example, provided herein are methods of treating a subject having a cancer that include: identifying a subject having a cancer cell that has one or more RET inhibitor resistance mutations; and administering to the identified subject a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the compound of Formula I or a pharmaceutically acceptable salt or solvate thereof is administered in combination with the first RET inhibitor. Also provided are methods of treating a subject identified as having a cancer cell that has one or more RET inhibitor resistance mutations that include administering to the subject a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the compound of Formula I or a pharmaceutically acceptable salt or solvate thereof is administered in combination with the first RET inhibitor. In some embodiments, the one or more RET inhibitor resistance mutations confer increased resistance to a cancer cell or tumor to treatment with the first RET inhibitor. In some embodiments, the one or more RET inhibitor resistance mutations include one or more RET inhibitor resistance mutations listed in Tables 3 and 4. For example, the one or more RET inhibitor resistance mutations can include a substitution at amino acid position 804, e.g., V804M, V804L, or V804E.

For example, provided herein are methods for treating a RET-associated cancer in a subject in need of such treatment, the method comprising (a) detecting a dysregulation of a RET gene, a RET kinase, or the expression or activity or level of any of the same in a sample from the subject; and (b) administering to the subject a therapeutically effective amount of a first RET inhibitor, wherein the first RET inhibitor is selected from the group consisting of: ((S)-4-(6-(4-(2-hydroxy-3-phenylpropanoyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(4-(2-(pyridin-2-yl)acetyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 4-(6-(4-(2,6-difluorobenzoyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile 2,2,2-trifluoroacetate; 4-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridin-4-yl)pyridin-2-yl)-N,N-diethylpiperazine-1-carboxamide; 1-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridin-4-yl)pyridin-2-yl)-N-(2-methoxy-3-methylbutyl)piperidine-4-carboxamide; 4-(6-(4-(2-(5-fluoropyridin-2-yl)acetyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile bis(2,2,2-trifluoroacetate); 4-(6-(4-(2,6-difluorobenzyl)piperazin-1-yl)pyridine-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 4-(6-(4-(2-methoxybenzyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(1-methyl-H-pyrazol-4-yl)-4-(6-(4-(pyridine-2-ylmethyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 4-(6-(4-((6-methoxypyridin-3-yl)methyl) piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the methods further comprise (after (b)) (c) determining whether a cancer cell in a sample obtained from the subject has at least one RET inhibitor resistance mutation; and (d) administering a compound of Formula I, or a pharmaceutically acceptable salt or solvate thereof as a monotherapy or in conjunction with another anticancer agent to the subject if the subject has a cancer cell that has at least one RET inhibitor resistance mutation; or (e) administering additional doses of the first RET inhibitor of step (b) to the subject if the subject has a cancer cell that does not have a RET inhibitor resistance mutation.

In some embodiments, provided herein are methods for treating a RET-associated cancer in a subject in need of such treatment, the method comprising (a) detecting a dysregulation of a RET gene, a RET kinase, or the expression or activity or level of any of the same in a sample from the subject; and (b) administering to the subject a therapeutically effective amount of a first RET inhibitor, wherein the first RET inhibitor is selected from the group consisting of: ((S)-4-(6-(4-(2-hydroxy-3-phenylpropanoyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(4-(2-(pyridin-2-yl)acetyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 4-(6-(4-(2,6-difluorobenzoyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile 2,2,2-trifluoroacetate; 4-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridin-4-yl)pyridin-2-yl)-N,N-diethylpiperazine-1-carboxamide; 1-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridin-4-yl)pyridin-2-yl)-N-(2-methoxy-3-methylbutyl)piperidine-4-carboxamide; 4-(6-(4-(2-(5-fluoropyridin-2-yl)acetyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile bis(2,2,2-trifluoroacetate); 4-(6-(4-(2,6-difluorobenzyl)piperazin-1-yl)pyridine-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 4-(6-(4-(2-methoxybenzyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(4-(pyridine-2-ylmethyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 4-(6-(4-((6-methoxypyridin-3-yl)methyl) piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the methods further comprise (after (b)) (c) determining whether a cancer cell in a sample obtained from the subject has at least one RET inhibitor resistance mutation; and (d) administering a compound of Formula I selected from i) Example No. 1-20; ii) Example No. 21-40; iii) Example No. 41-49; iv) Example No. 50-70; v) Example No. 71-90; vi) Example No. 91-110; vii) Example No. 111-121, or a pharmaceutically acceptable salt or solvate thereof as a monotherapy or in conjunction with another anticancer agent to the subject if the subject has a cancer cell that has at least one RET inhibitor resistance mutation; or (e) administering additional doses of the first RET inhibitor of step (b) to the subject if the subject has a cancer cell that does not have a RET inhibitor resistance mutation.

In some embodiments, provided herein are methods for treating a RET-associated cancer in a subject in need of such treatment, the method comprising (a) detecting one or more fusion proteins of Table 1 and/or one or more RET kinase protein point mutations/insertions/deletions of Tables 2 and 2a in a sample from the subject; and (b) administering to the subject a therapeutically effective amount of a first RET inhibitor, wherein the first RET inhibitor is selected from the group consisting of: ((S)-4-(6-(4-(2-hydroxy-3-phenylpropanoyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(4-(2-(pyridin-2-yl)acetyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 4-(6-(4-(2,6-difluorobenzoyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile 2,2,2-trifluoroacetate; 4-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridin-4-yl)pyridin-2-yl)-N,N-diethylpiperazine-1-carboxamide; 1-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridin-4-yl)pyridin-2-yl)-N-(2-methoxy-3-methylbutyl)piperidine-4-carboxamide; 4-(6-(4-(2-(5-fluoropyridin-2-yl)acetyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile bis(2,2,2-trifluoroacetate); 4-(6-(4-(2,6-difluorobenzyl)piperazin-1-yl)pyridine-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 4-(6-(4-(2-methoxybenzyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(4-(pyridine-2-ylmethyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 4-(6-(4-((6-methoxypyridin-3-yl)methyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the methods further comprise (after (b)) (c) determining whether a cancer cell in a sample obtained from the subject has at least one RET inhibitor resistance mutation of Tables 3 or 4; and (d) administering a compound of Formula I selected from i) Example No. 1-20; ii) Example No. 21-40; iii) Example No. 41-49; iv) Example No. 50-70; v) Example No. 71-90; vi) Example No. 91-110; vii) Example No. 111-121, or a pharmaceutically acceptable salt or solvate thereof as a monotherapy or in conjunction with another anticancer agent to the subject if the subject has a cancer cell that has at least one RET inhibitor resistance mutation; or (e) administering additional doses of the first RET inhibitor of step (b) to the subject if the subject has a cancer cell that does not have a RET inhibitor resistance mutation.

In some embodiments, provided herein are methods for treating a RET-associated cancer in a subject in need of such treatment, the method comprising (a) detecting the fusion protein KIF5B-RET in a sample from the subject; and (b) administering to the subject a therapeutically effective amount of a first RET inhibitor, wherein the first RET inhibitor is selected from the group consisting of ((S)-4-(6-(4-(2-hydroxy-3-phenylpropanoyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(4-(2-(pyridin-2-yl)acetyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 4-(6-(4-(2,6-difluorobenzoyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile 2,2,2-trifluoroacetate; 4-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridin-4-yl)pyridin-2-yl)-N,N-diethylpiperazine-1-carboxamide; 1-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridin-4-yl)pyridin-2-yl)-N-(2-methoxy-3-methylbutyl)piperidine-4-carboxamide; 4-(6-(4-(2-(5-fluoropyridin-2-yl)acetyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile bis(2,2,2-trifluoroacetate); 4-(6-(4-(2,6-difluorobenzyl)piperazin-1-yl)pyridine-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 4-(6-(4-(2-methoxybenzyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(4-(pyridine-2-ylmethyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 4-(6-(4-((6-methoxypyridin-3-yl)methyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the methods further comprise (after (b)) (c) determining whether a cancer cell in a sample obtained from the subject has the RET inhibitor resistance mutation V804M; and (d) administering a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof selected from the group consisting of a compound of Formula I selected from i) Example No. 1-20; ii) Example No. 21-40; iii) Example No. 41-49; iv) Example No. 50-70; v) Example No. 71-90; vi) Example No. 91-110; vii) Example No. 111-121, or a pharmaceutically acceptable salt or solvate thereof as a monotherapy or in conjunction with another anticancer agent to the subject if the subject has a cancer cell that has at least one RET inhibitor resistance mutation; or (e) administering additional doses of the first RET inhibitor of step (b) to the subject if the subject has a cancer cell that does not have a RET inhibitor resistance mutation.

As another example, provided herein are methods for treating a RET-associated cancer in a subject in need of such treatment, the method comprising (a) detecting a dysregulation of a RET gene, a RET kinase, or the expression or activity or level of any of the same in a sample from the subject; and (b) administering to the subject a therapeutically effective amount of a compound of Formula I, or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the methods further comprise (after (b)) (c) determining whether a cancer cell in a sample obtained from the subject has at least one RET inhibitor resistance mutation; and (d) administering a second RET inhibitor, wherein the second RET inhibitor is selected from the group consisting of: ((S)-4-(6-(4-(2-hydroxy-3-phenylpropanoyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(4-(2-(pyridin-2-yl)acetyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 4-(6-(4-(2,6-difluorobenzoyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-IH-pyrazol-4-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile 2,2,2-trifluoroacetate; 4-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridin-4-yl)pyridin-2-yl)-N,N-diethylpiperazine-1-carboxamide; 1-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridin-4-yl)pyridin-2-yl)-N-(2-methoxy-3-methylbutyl)piperidine-4-carboxamide; 4-(6-(4-(2-(5-fluoropyridin-2-yl)acetyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile bis(2,2,2-trifluoroacetate); 4-(6-(4-(2,6-difluorobenzyl)piperazin-1-yl)pyridine-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 4-(6-(4-(2-methoxybenzyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(1-methyl-IH-pyrazol-4-yl)-4-(6-(4-(pyridine-2-ylmethyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 4-(6-(4-((6-methoxypyridin-3-yl)methyl) piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; or a pharmaceutically acceptable salt or solvate thereof, as a monotherapy or in conjunction with another anticancer agent to the subject if the subject has a cancer cell that has at least one RET inhibitor resistance mutation; or (e) administering additional doses of the compound of Formula I or a pharmaceutically acceptable salt or solvate thereof of step (b) to the subject if the subject has a cancer cell that does not have a RET inhibitor resistance mutation. In some embodiments, provided herein are methods for treating a RET-associated cancer in a subject in need of such treatment, the method comprising (a) detecting a dysregulation of a RET gene, a RET kinase, or the expression or activity or level of any of the same in a sample from the subject; and (b) administering to the subject a therapeutically effective amount of a compound of Formula I selected from i) Example No. 1-20; ii) Example No. 21-40; iii) Example No. 41-49; iv) Example No. 50-70; v) Example No. 71-90; vi) Example No. 91-110; vii) Example No. 111-121, or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the methods further comprise (after (b)) (c) determining whether a cancer cell in a sample obtained from the subject has at least one RET inhibitor resistance mutation; and (d) administering a second RET inhibitor, wherein the second RET inhibitor is selected from the group consisting of: ((S)-4-(6-(4-(2-hydroxy-3-phenylpropanoyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(4-(2-(pyridin-2-yl)acetyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 4-(6-(4-(2,6-difluorobenzoyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile 2,2,2-trifluoroacetate; 4-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridin-4-yl)pyridin-2-yl)-N,N-diethylpiperazine-1-carboxamide; 1-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridin-4-yl)pyridin-2-yl)-N-(2-methoxy-3-methylbutyl)piperidine-4-carboxamide; 4-(6-(4-(2-(5-fluoropyridin-2-yl)acetyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile bis(2,2,2-trifluoroacetate); 4-(6-(4-(2,6-difluorobenzyl)piperazin-1-yl)pyridine-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 4-(6-(4-(2-methoxybenzyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(4-(pyridine-2-ylmethyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 4-(6-(4-((6-methoxypyridin-3-yl)methyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; or a pharmaceutically acceptable salt or solvate thereof, as a monotherapy or in conjunction with another anticancer agent to the subject if the subject has a cancer cell that has at least one RET inhibitor resistance mutation; or (e) administering additional doses of the compound of Formula I or a pharmaceutically acceptable salt or solvate thereof of step (b) to the subject if the subject has a cancer cell that does not have a RET inhibitor resistance mutation. In some embodiments, provided herein are methods for treating a RET-associated cancer in a subject in need of such treatment, the method comprising (a) detecting one or more fusion proteins of Table 1 and/or one or more RET kinase protein point mutations/insertions/deletions of Tables 2 and 2a in a sample from the subject; and (b) administering to the subject a therapeutically effective amount of a compound of Formula I selected i) Example No. 1-20; ii) Example No. 21-40; iii) Example No. 41-49; iv) Example No. 50-70; v) Example No. 71-90; vi) Example No. 91-110; vii) Example No. 111-121, or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the methods further comprise (after (b)) (c) determining whether a cancer cell in a sample obtained from the subject has at least one RET inhibitor resistance mutation of Tables 3 or 4; and (d) administering a second RET inhibitor, wherein the second RET inhibitor is selected from the group consisting of: ((S)-4-(6-(4-(2-hydroxy-3-phenylpropanoyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(4-(2-(pyridin-2-yl)acetyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 4-(6-(4-(2,6-difluorobenzoyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile 2,2,2-trifluoroacetate; 4-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridin-4-yl)pyridin-2-yl)-N,N-diethylpiperazine-1-carboxamide; 1-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridin-4-yl)pyridin-2-yl)-N-(2-methoxy-3-methylbutyl)piperidine-4-carboxamide; 4-(6-(4-(2-(5-fluoropyridin-2-yl)acetyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile bis(2,2,2-trifluoroacetate); 4-(6-(4-(2,6-difluorobenzyl)piperazin-1-yl)pyridine-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 4-(6-(4-(2-methoxybenzyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(4-(pyridine-2-ylmethyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 4-(6-(4-((6-methoxypyridin-3-yl)methyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; or a pharmaceutically acceptable salt or solvate thereof, as a monotherapy or in conjunction with another anticancer agent to the subject if the subject has a cancer cell that has at least one RET inhibitor resistance mutation; or (e) administering additional doses of the compound of Formula I or a pharmaceutically acceptable salt or solvate thereof of step (b) to the subject if the subject has a cancer cell that does not have a RET inhibitor resistance mutation. In some embodiments, provided herein are methods for treating a RET-associated cancer in a subject in need of such treatment, the method comprising (a) detecting the fusion protein KIF5B-RET in a sample from the subject; and (b) administering to the subject a therapeutically effective amount of a compound of Formula I selected from i) Example No. 1-20; ii) Example No. 21-40; iii) Example No. 41-49; iv) Example No. 50-70; v) Example No. 71-90; vi) Example No. 91-110; vii) Example No. 111-121, or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the methods further comprise (after (b)) (c) determining whether a cancer cell in a sample obtained from the subject has the RET inhibitor resistance mutation V804M; and (d) administering a second RET inhibitor, wherein the second RET inhibitor is selected from the group consisting of: ((S)-4-(6-(4-(2-hydroxy-3-phenylpropanoyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(4-(2-(pyridin-2-yl)acetyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 4-(6-(4-(2,6-difluorobenzoyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile 2,2,2-trifluoroacetate; 4-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridin-4-yl)pyridin-2-yl)-N,N-diethylpiperazine-1-carboxamide; 1-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridin-4-yl)pyridin-2-yl)-N-(2-methoxy-3-methylbutyl)piperidine-4-carboxamide; 4-(6-(4-(2-(5-fluoropyridin-2-yl)acetyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile bis(2,2,2-trifluoroacetate); 4-(6-(4-(2,6-difluorobenzyl)piperazin-1-yl)pyridine-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 4-(6-(4-(2-methoxybenzyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(4-(pyridine-2-ylmethyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 4-(6-(4-((6-methoxypyridin-3-yl)methyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; or a pharmaceutically acceptable salt or solvate thereof, as a monotherapy or in conjunction with another anticancer agent to the subject if the subject has a cancer cell that has at least one RET inhibitor resistance mutation; or (e) administering additional doses of the compound of Formula I or a pharmaceutically acceptable salt or solvate thereof of step (b) to the subject if the subject has a cancer cell that does not have a RET inhibitor resistance mutation.

In some embodiments, the presence of one or more RET inhibitor resistance mutations in a tumor causes the tumor to be more resistant to treatment with a first RET inhibitor. Methods useful when a RET inhibitor resistance mutation causes the tumor to be more resistant to treatment with a first RET inhibitor are described below. For example, provided herein are methods of treating a subject having a cancer that include: identifying a subject having a cancer cell that has one or more RET inhibitor resistance mutations; and administering to the identified subject a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the compound of Formula I or a pharmaceutically acceptable salt or solvate thereof is administered in combination with the first RET inhibitor. Also provided are methods of treating a subject identified as having a cancer cell that has one or more RET inhibitor resistance mutations that include administering to the subject a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the compound of Formula I or a pharmaceutically acceptable salt or solvate thereof is administered in combination with the first RET inhibitor. In some embodiments, the one or more RET inhibitor resistance mutations confer increased resistance to a cancer cell or tumor to treatment with the first RET inhibitor. In some embodiments, the one or more RET inhibitor resistance mutations include one or more RET inhibitor resistance mutations listed in Tables 3 and 4. For example, the one or more RET inhibitor resistance mutations can include a substitution at amino acid position 804, e.g., V804M, V804L, or V804E.

For example, provided herein are methods for treating a RET-associated cancer in a subject in need of such treatment, the method comprising (a) detecting a dysregulation of a RET gene, a RET kinase, or the expression or activity or level of any of the same in a sample from the subject; and (b) administering to the subject a therapeutically effective amount of a first RET inhibitor, wherein the first RET inhibitor is selected from the group consisting of: 4-(6-(4-benzylpiperazin-1-yl)pyridin-3-yl)-6-(2-morpholinoethoxy)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-hydroxyethoxy)-4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; (R)-6-(2-hydroxypropoxy)-4-(6-(4-((6-methoxypyridin-3-yl)methyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-hydroxy-2-methylpropoxy)-4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-methoxyethoxy)-4-(6-(4-((6-methoxypyridin-3-yl)methyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-hydroxy-2-methylpropoxy)-4-(6-(6-(6-methoxynicotinoyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-(dimethylamino)ethoxy)-4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)-6-(2-morpholinoethoxy)pyrazolo[1,5-a]pyridine-3-carbonitrile; 4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)-6-((1-methyl-1H-imidazol-4-yl)methoxy)pyrazolo[1,5-a]pyridine-3-carbonitrile; and 6-ethoxy-4-(5-(6-((5-fluoro-6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyrazin-2-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the methods further comprise (after (b)) (c) determining whether a cancer cell in a sample obtained from the subject has at least one RET inhibitor resistance mutation; and (d) administering a compound of Formula I, or a pharmaceutically acceptable salt or solvate thereof as a monotherapy or in conjunction with another anticancer agent to the subject if the subject has a cancer cell that has at least one RET inhibitor resistance mutation; or (e) administering additional doses of the first RET inhibitor of step (b) to the subject if the subject has a cancer cell that does not have a RET inhibitor resistance mutation.

In some embodiments, provided herein are methods for treating a RET-associated cancer in a subject in need of such treatment, the method comprising (a) detecting a dysregulation of a RET gene, a RET kinase, or the expression or activity or level of any of the same in a sample from the subject; and (b) administering to the subject a therapeutically effective amount of a first RET inhibitor, wherein the first RET inhibitor is selected from the group consisting of: 4-(6-(4-benzylpiperazin-1-yl)pyridin-3-yl)-6-(2-morpholinoethoxy)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-hydroxyethoxy)-4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; (R)-6-(2-hydroxypropoxy)-4-(6-(4-((6-methoxypyridin-3-yl)methyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-hydroxy-2-methylpropoxy)-4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-methoxyethoxy)-4-(6-(4-((6-methoxypyridin-3-yl)methyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-hydroxy-2-methylpropoxy)-4-(6-(6-(6-methoxynicotinoyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-(dimethylamino)ethoxy)-4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)-6-(2-morpholinoethoxy)pyrazolo[1,5-a]pyridine-3-carbonitrile; 4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)-6-((1-methyl-1H-imidazol-4-yl)methoxy)pyrazolo[1,5-a]pyridine-3-carbonitrile; and 6-ethoxy-4-(5-(6-((5-fluoro-6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyrazin-2-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the methods further comprise (after (b)) (c) determining whether a cancer cell in a sample obtained from the subject has at least one RET inhibitor resistance mutation; and (d) administering a compound of Formula I selected from i) Example No. 1-20; ii) Example No. 21-40; iii) Example No. 41-49; iv) Example No. 50-70; v) Example No. 71-90; vi) Example No. 91-110; vii) Example No. 111-121, or a pharmaceutically acceptable salt or solvate thereof as a monotherapy or in conjunction with another anticancer agent to the subject if the subject has a cancer cell that has at least one RET inhibitor resistance mutation; or (e) administering additional doses of the first RET inhibitor of step (b) to the subject if the subject has a cancer cell that does not have a RET inhibitor resistance mutation.

In some embodiments, provided herein are methods for treating a RET-associated cancer in a subject in need of such treatment, the method comprising (a) detecting one or more fusion proteins of Table 1 and/or one or more RET kinase protein point mutations/insertions/deletions of Tables 2 and 2a in a sample from the subject; and (b) administering to the subject a therapeutically effective amount of a first RET inhibitor, wherein the first RET inhibitor is selected from the group consisting of: 4-(6-(4-benzylpiperazin-1-yl)pyridin-3-yl)-6-(2-morpholinoethoxy)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-hydroxyethoxy)-4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; (R)-6-(2-hydroxypropoxy)-4-(6-(4-((6-methoxypyridin-3-yl)methyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-hydroxy-2-methyl propoxy)-4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-methoxyethoxy)-4-(6-(4-((6-methoxypyridin-3-yl)methyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-hydroxy-2-methylpropoxy)-4-(6-(6-(6-methoxynicotinoyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-(dimethylamino)ethoxy)-4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)-6-(2-morpholinoethoxy)pyrazolo[1,5-a]pyridine-3-carbonitrile; 4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)-6-((1-methyl-1H-imidazol-4-yl)methoxy)pyrazolo[1,5-a]pyridine-3-carbonitrile; and 6-ethoxy-4-(5-(6-((5-fluoro-6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyrazin-2-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the methods further comprise (after (b)) (c) determining whether a cancer cell in a sample obtained from the subject has at least one RET inhibitor resistance mutation of Tables 3 or 4; and (d) administering a compound of Formula I selected from i) Example No. 1-20; ii) Example No. 21-40; iii) Example No. 41-49; iv) Example No. 50-70; v) Example No. 71-90; vi) Example No. 91-110; vii) Example No. 111-121, or a pharmaceutically acceptable salt or solvate thereof as a monotherapy or in conjunction with another anticancer agent to the subject if the subject has a cancer cell that has at least one RET inhibitor resistance mutation; or (e) administering additional doses of the first RET inhibitor of step (b) to the subject if the subject has a cancer cell that does not have a RET inhibitor resistance mutation.

In some embodiments, provided herein are methods for treating a RET-associated cancer in a subject in need of such treatment, the method comprising (a) detecting the fusion protein KIF5B-RET in a sample from the subject; and (b) administering to the subject a therapeutically effective amount of a first RET inhibitor, wherein the first RET inhibitor is selected from the group consisting of 4-(6-(4-benzylpiperazin-1-yl)pyridin-3-yl)-6-(2-morpholinoethoxy)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-hydroxyethoxy)-4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; (R)-6-(2-hydroxypropoxy)-4-(6-(4-((6-methoxypyridin-3-yl)methyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-hydroxy-2-methyl propoxy)-4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-methoxyethoxy)-4-(6-(4-((6-methoxypyridin-3-yl)methyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-hydroxy-2-methylpropoxy)-4-(6-(6-(6-methoxynicotinoyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-(dimethylamino)ethoxy)-4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)-6-(2-morpholinoethoxy)pyrazolo[1,5-a]pyridine-3-carbonitrile; 4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)-6-((1-methyl-1H-imidazol-4-yl)methoxy)pyrazolo[1,5-a]pyridine-3-carbonitrile; and 6-ethoxy-4-(5-(6-((5-fluoro-6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyrazin-2-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the methods further comprise (after (b)) (c) determining whether a cancer cell in a sample obtained from the subject has the RET inhibitor resistance mutation V804M; and (d) administering a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof selected from the group consisting of a compound of Formula I selected from i) Example No. 1-20; ii) Example No. 21-40; iii) Example No. 41-49; iv) Example No. 50-70; v) Example No. 71-90; vi) Example No. 91-110; vii) Example No. 111-121, or a pharmaceutically acceptable salt or solvate thereof as a monotherapy or in conjunction with another anticancer agent to the subject if the subject has a cancer cell that has at least one RET inhibitor resistance mutation; or (e) administering additional doses of the first RET inhibitor of step (b) to the subject if the subject has a cancer cell that does not have a RET inhibitor resistance mutation.

As another example, provided herein are methods for treating a RET-associated cancer in a subject in need of such treatment, the method comprising (a) detecting a dysregulation of a RET gene, a RET kinase, or the expression or activity or level of any of the same in a sample from the subject; and (b) administering to the subject a therapeutically effective amount of a compound of Formula I, or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the methods further comprise (after (b)) (c) determining whether a cancer cell in a sample obtained from the subject has at least one RET inhibitor resistance mutation; and (d) administering a second RET inhibitor, wherein the second RET inhibitor is selected from the group consisting of: 4-(6-(4-benzylpiperazin-1-yl)pyridin-3-yl)-6-(2-morpholinoethoxy)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-hydroxyethoxy)-4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; (R)-6-(2-hydroxypropoxy)-4-(6-(4-((6-methoxypyridin-3-yl)methyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-hydroxy-2-methylpropoxy)-4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-methoxyethoxy)-4-(6-(4-((6-methoxypyridin-3-yl)methyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-hydroxy-2-methylpropoxy)-4-(6-(6-(6-methoxynicotinoyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-(dimethylamino)ethoxy)-4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)-6-(2-morpholinoethoxy)pyrazolo[1,5-a]pyridine-3-carbonitrile; 4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)-6-((1-methyl-1H-imidazol-4-yl)methoxy)pyrazolo[1,5-a]pyridine-3-carbonitrile; and 6-ethoxy-4-(5-(6-((5-fluoro-6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyrazin-2-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; or a pharmaceutically acceptable salt or solvate thereof, as a monotherapy or in conjunction with another anticancer agent to the subject if the subject has a cancer cell that has at least one RET inhibitor resistance mutation; or (e) administering additional doses of the compound of Formula I or a pharmaceutically acceptable salt or solvate thereof of step (b) to the subject if the subject has a cancer cell that does not have a RET inhibitor resistance mutation. In some embodiments, provided herein are methods for treating a RET-associated cancer in a subject in need of such treatment, the method comprising (a) detecting a dysregulation of a RET gene, a RET kinase, or the expression or activity or level of any of the same in a sample from the subject; and (b) administering to the subject a therapeutically effective amount of a compound of Formula I selected from i) Example No. 1-20; ii) Example No. 21-40; iii) Example No. 41-49; iv) Example No. 50-70; v) Example No. 71-90; vi) Example No. 91-110; vii) Example No. 111-121, or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the methods further comprise (after (b)) (c) determining whether a cancer cell in a sample obtained from the subject has at least one RET inhibitor resistance mutation; and (d) administering a second RET inhibitor, wherein the second RET inhibitor is selected from the group consisting of: 4-(6-(4-benzylpiperazin-1-yl)pyridin-3-yl)-6-(2-morpholinoethoxy)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-hydroxyethoxy)-4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; (R)-6-(2-hydroxypropoxy)-4-(6-(4-((6-methoxypyridin-3-yl)methyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-hydroxy-2-methylpropoxy)-4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-methoxyethoxy)-4-(6-(4-((6-methoxypyridin-3-yl)methyl) piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-hydroxy-2-methylpropoxy)-4-(6-(6-(6-methoxynicotinoyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-(dimethylamino)ethoxy)-4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)-6-(2-morpholinoethoxy)pyrazolo[1,5-a]pyridine-3-carbonitrile; 4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)-6-((1-methyl-1H-imidazol-4-yl)methoxy)pyrazolo[1,5-a]pyridine-3-carbonitrile; and 6-ethoxy-4-(5-(6-((5-fluoro-6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyrazin-2-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; or a pharmaceutically acceptable salt or solvate thereof, as a monotherapy or in conjunction with another anticancer agent to the subject if the subject has a cancer cell that has at least one RET inhibitor resistance mutation; or (e) administering additional doses of the compound of Formula I or a pharmaceutically acceptable salt or solvate thereof of step (b) to the subject if the subject has a cancer cell that does not have a RET inhibitor resistance mutation. In some embodiments, provided herein are methods for treating a RET-associated cancer in a subject in need of such treatment, the method comprising (a) detecting one or more fusion proteins of Table 1 and/or one or more RET kinase protein point mutations/insertions/deletions of Tables 2 and 2a in a sample from the subject; and (b) administering to the subject a therapeutically effective amount of a compound of Formula I selected from i) Example No. 1-20; ii) Example No. 21-40; iii) Example No. 41-49; iv) Example No. 50-70; v) Example No. 71-90; vi) Example No. 91-110; vii) Example No. 111-121, or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the methods further comprise (after (b)) (c) determining whether a cancer cell in a sample obtained from the subject has at least one RET inhibitor resistance mutation of Tables 3 or 4; and (d) administering a second RET inhibitor, wherein the second RET inhibitor is selected from the group consisting of: 4-(6-(4-benzylpiperazin-1-yl)pyridin-3-yl)-6-(2-morpholinoethoxy)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-hydroxyethoxy)-4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; (R)-6-(2-hydroxypropoxy)-4-(6-(4-((6-methoxypyridin-3-yl)methyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-hydroxy-2-methylpropoxy)-4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-methoxyethoxy)-4-(6-(4-((6-methoxypyridin-3-yl)methyl) piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-hydroxy-2-methylpropoxy)-4-(6-(6-(6-methoxynicotinoyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-(dimethylamino)ethoxy)-4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)-6-(2-morpholinoethoxy)pyrazolo[1,5-a]pyridine-3-carbonitrile; 4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)-6-((1-methyl-1H-imidazol-4-yl)methoxy)pyrazolo[1,5-a]pyridine-3-carbonitrile; and 6-ethoxy-4-(5-(6-((5-fluoro-6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyrazin-2-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; or a pharmaceutically acceptable salt or solvate thereof, as a monotherapy or in conjunction with another anticancer agent to the subject if the subject has a cancer cell that has at least one RET inhibitor resistance mutation; or (e) administering additional doses of the compound of Formula I or a pharmaceutically acceptable salt or solvate thereof of step (b) to the subject if the subject has a cancer cell that does not have a RET inhibitor resistance mutation. In some embodiments, provided herein are methods for treating a RET-associated cancer in a subject in need of such treatment, the method comprising (a) detecting the fusion protein KIF5B-RET in a sample from the subject; and (b) administering to the subject a therapeutically effective amount of a compound of Formula I selected from i) Example No. 1-20; ii) Example No. 21-40; iii) Example No. 41-49; iv) Example No. 50-70; v) Example No. 71-90; vi) Example No. 91-110; vii) Example No. 111-121, or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the methods further comprise (after (b)) (c) determining whether a cancer cell in a sample obtained from the subject has the RET inhibitor resistance mutation V804M; and (d) administering a second RET inhibitor, wherein the second RET inhibitor is selected from the group consisting of: 4-(6-(4-benzylpiperazin-1-yl)pyridin-3-yl)-6-(2-morpholinoethoxy)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-hydroxyethoxy)-4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; (R)-6-(2-hydroxypropoxy)-4-(6-(4-((6-methoxypyridin-3-yl)methyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-hydroxy-2-methyl propoxy)-4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-methoxyethoxy)-4-(6-(4-((6-methoxypyridin-3-yl)methyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-hydroxy-2-methylpropoxy)-4-(6-(6-(6-methoxynicotinoyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-(dimethylamino)ethoxy)-4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)-6-(2-morpholinoethoxy)pyrazolo[1,5-a]pyridine-3-carbonitrile; 4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)-6-((1-methyl-1H-imidazol-4-yl)methoxy)pyrazolo[1,5-a]pyridine-3-carbonitrile; and 6-ethoxy-4-(5-(6-((5-fluoro-6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyrazin-2-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; or a pharmaceutically acceptable salt or solvate thereof, as a monotherapy or in conjunction with another anticancer agent to the subject if the subject has a cancer cell that has at least one RET inhibitor resistance mutation; or (e) administering additional doses of the compound of Formula I or a pharmaceutically acceptable salt or solvate thereof of step (b) to the subject if the subject has a cancer cell that does not have a RET inhibitor resistance mutation.

In some embodiments, the presence of one or more RET inhibitor resistance mutations in a tumor causes the tumor to be more resistant to treatment with a first RET inhibitor. Methods useful when a RET inhibitor resistance mutation causes the tumor to be more resistant to treatment with a first RET inhibitor are described below. For example, provided herein are methods of treating a subject having a cancer that include: identifying a subject having a cancer cell that has one or more RET inhibitor resistance mutations; and administering to the identified subject a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the compound of Formula I or a pharmaceutically acceptable salt or solvate thereof is administered in combination with the first RET inhibitor. Also provided are methods of treating a subject identified as having a cancer cell that has one or more RET inhibitor resistance mutations that include administering to the subject a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the compound of Formula I or a pharmaceutically acceptable salt or solvate thereof is administered in combination with the first RET inhibitor. In some embodiments, the one or more RET inhibitor resistance mutations confer increased resistance to a cancer cell or tumor to treatment with the first RET inhibitor. In some embodiments, the one or more RET inhibitor resistance mutations include one or more RET inhibitor resistance mutations listed in Tables 3 and 4. For example, the one or more RET inhibitor resistance mutations can include a substitution at amino acid position 804, e.g., V804M, V804L, or V804E.

For example, provided herein are methods for treating a RET-associated cancer in a subject in need of such treatment, the method comprising (a) detecting a dysregulation of a RET gene, a RET kinase, or the expression or activity or level of any of the same in a sample from the subject; and (b) administering to the subject a therapeutically effective amount of a first RET inhibitor, wherein the first RET inhibitor is selected from the group consisting of: N-(1-(5-(3-cyano-6-(2-hydroxy-2-methylpropoxy)pyrazolo[1,5-a]pyridin-4-yl)pyridin-2-yl)-4-methylpiperidin-4-yl)benzamide; 6-ethoxy-4-(6-(4-hydroxy-4-(pyridin-2-ylmethyl)piperidin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-hydroxy-2-methylpropoxy)-4-(6-(3-(pyridin-2-yloxy)azetidin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-hydroxy-2-methylpropoxy)-4-(6-(4-((6-methoxypyridazin-3-yl)oxy)piperidin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; (S)-6-(2-hydroxy-2-methylpropoxy)-4-(6-(3-(pyridin-2-yloxy)pyrrolidin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; N-(1-(5-(3-cyano-6-((3-fluoro-1-methyl azetidin-3-yl)methoxy)pyrazolo[1,5-a]pyridin-4-yl)pyridin-2-yl)-4-methylpiperidin-4-yl)-5-fluoro-2-methylbenzamide; 3-chloro-N-(1-(5-(3-cyano-6-((3-fluoro-1-methylazetidin-3-yl)methoxy)pyrazolo[1,5-a]pyridin-4-yl)pyridin-2-yl)-4-methylpiperidin-4-yl)picolinamide; N-((3S,4S)-1-(5-(3-cyano-6-ethoxypyrazolo[1,5-a]pyridin-4-yl)pyridin-2-yl)-3-hydroxypiperidin-4-yl)-3-methylbutanamide; 6-(2-hydroxy-2-methylpropoxy)-4-(6-(4-hydroxy-4-(pyridin-2-ylmethyl)piperidin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; and 3-chloro-N-((3S,4S)-1-(5-(3-cyano-6-ethoxypyrazolo[1,5-a]pyridin-4-yl)pyrazin-2-yl)-3-hydroxypiperidin-4-yl)picolinamide; or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the methods further comprise (after (b)) (c) determining whether a cancer cell in a sample obtained from the subject has at least one RET inhibitor resistance mutation; and (d) administering a compound of Formula I, or a pharmaceutically acceptable salt or solvate thereof as a monotherapy or in conjunction with another anticancer agent to the subject if the subject has a cancer cell that has at least one RET inhibitor resistance mutation; or (e) administering additional doses of the first RET inhibitor of step (b) to the subject if the subject has a cancer cell that does not have a RET inhibitor resistance mutation.

In some embodiments, provided herein are methods for treating a RET-associated cancer in a subject in need of such treatment, the method comprising (a) detecting a dysregulation of a RET gene, a RET kinase, or the expression or activity or level of any of the same in a sample from the subject; and (b) administering to the subject a therapeutically effective amount of a first RET inhibitor, wherein the first RET inhibitor is selected from the group consisting of: N-(1-(5-(3-cyano-6-(2-hydroxy-2-methylpropoxy)pyrazolo[1,5-a]pyridin-4-yl)pyridin-2-yl)-4-methylpiperidin-4-yl)benzamide; 6-ethoxy-4-(6-(4-hydroxy-4-(pyridin-2-ylmethyl)piperidin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-hydroxy-2-methylpropoxy)-4-(6-(3-(pyridin-2-yloxy)azetidin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-hydroxy-2-methylpropoxy)-4-(6-(4-((6-methoxypyridazin-3-yl)oxy)piperidin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; (S)-6-(2-hydroxy-2-methylpropoxy)-4-(6-(3-(pyridin-2-yloxy)pyrrolidin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; N-(1-(5-(3-cyano-6-((3-fluoro-1-methyl azetidin-3-yl)methoxy)pyrazolo[1,5-a]pyridin-4-yl)pyridin-2-yl)-4-methylpiperidin-4-yl)-5-fluoro-2-methylbenzamide; 3-chloro-N-(1-(5-(3-cyano-6-((3-fluoro-1-methylazetidin-3-yl)methoxy)pyrazolo[1,5-a]pyridin-4-yl)pyridin-2-yl)-4-methylpiperidin-4-yl)picolinamide; N-((3S,4S)-1-(5-(3-cyano-6-ethoxypyrazolo[1,5-a]pyridin-4-yl)pyridin-2-yl)-3-hydroxypiperidin-4-yl)-3-methylbutanamide; 6-(2-hydroxy-2-methylpropoxy)-4-(6-(4-hydroxy-4-(pyridin-2-ylmethyl)piperidin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; and 3-chloro-N-((3S,4S)-1-(5-(3-cyano-6-ethoxypyrazolo[1,5-a]pyridin-4-yl)pyrazin-2-yl)-3-hydroxypiperidin-4-yl)picolinamide; or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the methods further comprise (after (b)) (c) determining whether a cancer cell in a sample obtained from the subject has at least one RET inhibitor resistance mutation; and (d) administering a compound of Formula I selected from i) Example No. 1-20; ii) Example No. 21-40; iii) Example No. 41-49; iv) Example No. 50-70; v) Example No. 71-90; vi) Example No. 91-110; vii) Example No. 111-121, or a pharmaceutically acceptable salt or solvate thereof as a monotherapy or in conjunction with another anticancer agent to the subject if the subject has a cancer cell that has at least one RET inhibitor resistance mutation; or (e) administering additional doses of the first RET inhibitor of step (b) to the subject if the subject has a cancer cell that does not have a RET inhibitor resistance mutation.

In some embodiments, provided herein are methods for treating a RET-associated cancer in a subject in need of such treatment, the method comprising (a) detecting one or more fusion proteins of Table 1 and/or one or more RET kinase protein point mutations/insertions/deletions of Tables 2 and 2a in a sample from the subject; and (b) administering to the subject a therapeutically effective amount of a first RET inhibitor, wherein the first RET inhibitor is selected from the group consisting of: N-(1-(5-(3-cyano-6-(2-hydroxy-2-methylpropoxy)pyrazolo[1,5-a]pyridin-4-yl)pyridin-2-yl)-4-methylpiperidin-4-yl)benzamide; 6-ethoxy-4-(6-(4-hydroxy-4-(pyridin-2-ylmethyl)piperidin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-hydroxy-2-methylpropoxy)-4-(6-(3-(pyridin-2-yloxy)azetidin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-hydroxy-2-methylpropoxy)-4-(6-(4-((6-methoxypyridazin-3-yl)oxy)piperidin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; (S)-6-(2-hydroxy-2-methylpropoxy)-4-(6-(3-(pyridin-2-yloxy)pyrrolidin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; N-(1-(5-(3-cyano-6-((3-fluoro-1-methylazetidin-3-yl)methoxy)pyrazolo[1,5-a]pyridin-4-yl)pyridin-2-yl)-4-methylpiperidin-4-yl)-5-fluoro-2-methylbenzamide; 3-chloro-N-(1-(5-(3-cyano-6-((3-fluoro-1-methylazetidin-3-yl)methoxy)pyrazolo[1,5-a]pyridin-4-yl)pyridin-2-yl)-4-methylpiperidin-4-yl)picolinamide; N-((3S,4S)-1-(5-(3-cyano-6-ethoxypyrazolo[1,5-a]pyridin-4-yl)pyridin-2-yl)-3-hydroxypiperidin-4-yl)-3-methylbutanamide; 6-(2-hydroxy-2-methylpropoxy)-4-(6-(4-hydroxy-4-(pyridin-2-ylmethyl)piperidin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; and 3-chloro-N-((3S,4S)-1-(5-(3-cyano-6-ethoxypyrazolo[1,5-a]pyridin-4-yl)pyrazin-2-yl)-3-hydroxypiperidin-4-yl)picolinamide; or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the methods further comprise (after (b)) (c) determining whether a cancer cell in a sample obtained from the subject has at least one RET inhibitor resistance mutation of Tables 3 or 4; and (d) administering a compound of Formula I selected from i) Example No. 1-20; ii) Example No. 21-40; iii) Example No. 41-49; iv) Example No. 50-70; v) Example No. 71-90; vi) Example No. 91-110; vii) Example No. 111-121, or a pharmaceutically acceptable salt or solvate thereof as a monotherapy or in conjunction with another anticancer agent to the subject if the subject has a cancer cell that has at least one RET inhibitor resistance mutation; or (e) administering additional doses of the first RET inhibitor of step (b) to the subject if the subject has a cancer cell that does not have a RET inhibitor resistance mutation.

In some embodiments, provided herein are methods for treating a RET-associated cancer in a subject in need of such treatment, the method comprising (a) detecting the fusion protein KIF5B-RET in a sample from the subject; and (b) administering to the subject a therapeutically effective amount of a first RET inhibitor, wherein the first RET inhibitor is selected from the group consisting of: N-(1-(5-(3-cyano-6-(2-hydroxy-2-methylpropoxy)pyrazolo[1,5-a]pyridin-4-yl)pyridin-2-yl)-4-methylpiperidin-4-yl)benzamide; 6-ethoxy-4-(6-(4-hydroxy-4-(pyridin-2-ylmethyl)piperidin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-hydroxy-2-methylpropoxy)-4-(6-(3-(pyridin-2-yloxy)azetidin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-hydroxy-2-methylpropoxy)-4-(6-(4-((6-methoxypyridazin-3-yl)oxy)piperidin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; (S)-6-(2-hydroxy-2-methylpropoxy)-4-(6-(3-(pyridin-2-yloxy)pyrrolidin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; N-(1-(5-(3-cyano-6-((3-fluoro-1-methylazetidin-3-yl)methoxy)pyrazolo[1,5-a]pyridin-4-yl)pyridin-2-yl)-4-methylpiperidin-4-yl)-5-fluoro-2-methylbenzamide; 3-chloro-N-(1-(5-(3-cyano-6-((3-fluoro-1-methylazetidin-3-yl)methoxy)pyrazolo[1,5-a]pyridin-4-yl)pyridin-2-yl)-4-methylpiperidin-4-yl)picolinamide; N-((3S,4S)-1-(5-(3-cyano-6-ethoxypyrazolo[1,5-a]pyridin-4-yl)pyridin-2-yl)-3-hydroxypiperidin-4-yl)-3-methylbutanamide; 6-(2-hydroxy-2-methylpropoxy)-4-(6-(4-hydroxy-4-(pyridin-2-ylmethyl)piperidin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; and 3-chloro-N-((3S,4S)-1-(5-(3-cyano-6-ethoxypyrazolo[1,5-a]pyridin-4-yl)pyrazin-2-yl)-3-hydroxypiperidin-4-yl)picolinamide; or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the methods further comprise (after (b)) (c) determining whether a cancer cell in a sample obtained from the subject has the RET inhibitor resistance mutation V804M; and (d) administering a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof selected from the group consisting of a compound of Formula I selected from i) Example No. 1-20; ii) Example No. 21-40; iii) Example No. 41-49; iv) Example No. 50-70; v) Example No. 71-90; vi) Example No. 91-110; vii) Example No. 111-121, or a pharmaceutically acceptable salt or solvate thereof as a monotherapy or in conjunction with another anticancer agent to the subject if the subject has a cancer cell that has at least one RET inhibitor resistance mutation; or (e) administering additional doses of the first RET inhibitor of step (b) to the subject if the subject has a cancer cell that does not have a RET inhibitor resistance mutation.

As another example, provided herein are methods for treating a RET-associated cancer in a subject in need of such treatment, the method comprising (a) detecting a dysregulation of a RET gene, a RET kinase, or the expression or activity or level of any of the same in a sample from the subject; and (b) administering to the subject a therapeutically effective amount of a compound of Formula I, or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the methods further comprise (after (b)) (c) determining whether a cancer cell in a sample obtained from the subject has at least one RET inhibitor resistance mutation; and (d) administering a second RET inhibitor, wherein the second RET inhibitor is selected from the group consisting of: N-(1-(5-(3-cyano-6-(2-hydroxy-2-methylpropoxy)pyrazolo[1,5-a]pyridin-4-yl)pyridin-2-yl)-4-methylpiperidin-4-yl)benzamide; 6-ethoxy-4-(6-(4-hydroxy-4-(pyridin-2-ylmethyl)piperidin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-hydroxy-2-methylpropoxy)-4-(6-(3-(pyridin-2-yloxy)azetidin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-hydroxy-2-methylpropoxy)-4-(6-(4-((6-methoxypyridazin-3-yl)oxy)piperidin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; (S)-6-(2-hydroxy-2-methylpropoxy)-4-(6-(3-(pyridin-2-yloxy)pyrrolidin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; N-(1-(5-(3-cyano-6-((3-fluoro-1-methyl azetidin-3-yl)methoxy)pyrazolo[1,5-a]pyridin-4-yl)pyridin-2-yl)-4-methylpiperidin-4-yl)-5-fluoro-2-methylbenzamide; 3-chloro-N-(1-(5-(3-cyano-6-((3-fluoro-1-methylazetidin-3-yl)methoxy)pyrazolo[1,5-a]pyridin-4-yl)pyridin-2-yl)-4-methylpiperidin-4-yl)picolinamide; N-((3S,4S)-1-(5-(3-cyano-6-ethoxypyrazolo[1,5-a]pyridin-4-yl)pyridin-2-yl)-3-hydroxypiperidin-4-yl)-3-methylbutanamide; 6-(2-hydroxy-2-methylpropoxy)-4-(6-(4-hydroxy-4-(pyridin-2-ylmethyl)piperidin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; and 3-chloro-N-((3S,4S)-1-(5-(3-cyano-6-ethoxypyrazolo[1,5-a]pyridin-4-yl)pyrazin-2-yl)-3-hydroxypiperidin-4-yl)picolinamide; or a pharmaceutically acceptable salt or solvate thereof, as a monotherapy or in conjunction with another anticancer agent to the subject if the subject has a cancer cell that has at least one RET inhibitor resistance mutation; or (e) administering additional doses of the compound of Formula I or a pharmaceutically acceptable salt or solvate thereof of step (b) to the subject if the subject has a cancer cell that does not have a RET inhibitor resistance mutation. In some embodiments, provided herein are methods for treating a RET-associated cancer in a subject in need of such treatment, the method comprising (a) detecting a dysregulation of a RET gene, a RET kinase, or the expression or activity or level of any of the same in a sample from the subject; and (b) administering to the subject a therapeutically effective amount of a compound of Formula I selected from i) Example No. 1-20; ii) Example No. 21-40; iii) Example No. 41-49; iv) Example No. 50-70; v) Example No. 71-90; vi) Example No. 91-110; vii) Example No. 111-121, or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the methods further comprise (after (b)) (c) determining whether a cancer cell in a sample obtained from the subject has at least one RET inhibitor resistance mutation; and (d) administering a second RET inhibitor, wherein the second RET inhibitor is selected from the group consisting of: N-(1-(5-(3-cyano-6-(2-hydroxy-2-methylpropoxy)pyrazolo[1,5-a]pyridin-4-yl)pyridin-2-yl)-4-methylpiperidin-4-yl)benzamide; 6-ethoxy-4-(6-(4-hydroxy-4-(pyridin-2-ylmethyl)piperidin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-hydroxy-2-methylpropoxy)-4-(6-(3-(pyridin-2-yloxy)azetidin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-hydroxy-2-methylpropoxy)-4-(6-(4-((6-methoxypyridazin-3-yl)oxy)piperidin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; (S)-6-(2-hydroxy-2-methylpropoxy)-4-(6-(3-(pyridin-2-yloxy)pyrrolidin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; N-(1-(5-(3-cyano-6-((3-fluoro-1-methylazetidin-3-yl)methoxy)pyrazolo[1,5-a]pyridin-4-yl)pyridin-2-yl)-4-methylpiperidin-4-yl)-5-fluoro-2-methylbenzamide; 3-chloro-N-(1-(5-(3-cyano-6-((3-fluoro-1-methylazetidin-3-yl)methoxy)pyrazolo[1,5-a]pyridin-4-yl)pyridin-2-yl)-4-methylpiperidin-4-yl)picolinamide; N-((3S,4S)-1-(5-(3-cyano-6-ethoxypyrazolo[1,5-a]pyridin-4-yl)pyridin-2-yl)-3-hydroxypiperidin-4-yl)-3-methylbutanamide; 6-(2-hydroxy-2-methylpropoxy)-4-(6-(4-hydroxy-4-(pyridin-2-ylmethyl)piperidin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; and 3-chloro-N-((3S,4S)-1-(5-(3-cyano-6-ethoxypyrazolo[1,5-a]pyridin-4-yl)pyrazin-2-yl)-3-hydroxypiperidin-4-yl)picolinamide; or a pharmaceutically acceptable salt or solvate thereof, as a monotherapy or in conjunction with another anticancer agent to the subject if the subject has a cancer cell that has at least one RET inhibitor resistance mutation; or (e) administering additional doses of the compound of Formula I or a pharmaceutically acceptable salt or solvate thereof of step (b) to the subject if the subject has a cancer cell that does not have a RET inhibitor resistance mutation. In some embodiments, provided herein are methods for treating a RET-associated cancer in a subject in need of such treatment, the method comprising (a) detecting one or more fusion proteins of Table 1 and/or one or more RET kinase protein point mutations/insertions/deletions of Tables 2 and 2a in a sample from the subject; and (b) administering to the subject a therapeutically effective amount of a compound of Formula I selected from i) Example No. 1-20; ii) Example No. 21-40; iii) Example No. 41-49; iv) Example No. 50-70; v) Example No. 71-90; vi) Example No. 91-110; vii) Example No. 111-121, or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the methods further comprise (after (b)) (c) determining whether a cancer cell in a sample obtained from the subject has at least one RET inhibitor resistance mutation of Tables 3 or 4; and (d) administering a second RET inhibitor, wherein the second RET inhibitor is selected from the group consisting of: N-(1-(5-(3-cyano-6-(2-hydroxy-2-methyl propoxy)pyrazolo[1,5-a]pyridin-4-yl)pyridin-2-yl)-4-methyl piperidin-4-yl)benzamide; 6-ethoxy-4-(6-(4-hydroxy-4-(pyridin-2-ylmethyl)piperidin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-hydroxy-2-methylpropoxy)-4-(6-(3-(pyridin-2-yloxy)azetidin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-hydroxy-2-methylpropoxy)-4-(6-(4-((6-methoxypyridazin-3-yl)oxy)piperidin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; (S)-6-(2-hydroxy-2-methylpropoxy)-4-(6-(3-(pyridin-2-yloxy)pyrrolidin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; N-(1-(5-(3-cyano-6-((3-fluoro-1-methylazetidin-3-yl)methoxy)pyrazolo[1,5-a]pyridin-4-yl)pyridin-2-yl)-4-methylpiperidin-4-yl)-5-fluoro-2-methylbenzamide; 3-chloro-N-(1-(5-(3-cyano-6-((3-fluoro-1-methylazetidin-3-yl)methoxy)pyrazolo[1,5-a]pyridin-4-yl)pyridin-2-yl)-4-methylpiperidin-4-yl)picolinamide; N-((3S,4S)-1-(5-(3-cyano-6-ethoxypyrazolo[1,5-a]pyridin-4-yl)pyridin-2-yl)-3-hydroxypiperidin-4-yl)-3-methylbutanamide; 6-(2-hydroxy-2-methylpropoxy)-4-(6-(4-hydroxy-4-(pyridin-2-ylmethyl)piperidin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; and 3-chloro-N-((3S,4S)-1-(5-(3-cyano-6-ethoxypyrazolo[1,5-a]pyridin-4-yl)pyrazin-2-yl)-3-hydroxypiperidin-4-yl)picolinamide; or a pharmaceutically acceptable salt or solvate thereof, as a monotherapy or in conjunction with another anticancer agent to the subject if the subject has a cancer cell that has at least one RET inhibitor resistance mutation; or (e) administering additional doses of the compound of Formula I or a pharmaceutically acceptable salt or solvate thereof of step (b) to the subject if the subject has a cancer cell that does not have a RET inhibitor resistance mutation. In some embodiments, provided herein are methods for treating a RET-associated cancer in a subject in need of such treatment, the method comprising (a) detecting the fusion protein KIF5B-RET in a sample from the subject; and (b) administering to the subject a therapeutically effective amount of a compound of Formula I selected from i) Example No. 1-20; ii) Example No. 21-40; iii) Example No. 41-49; iv) Example No. 50-70; v) Example No. 71-90; vi) Example No. 91-110; vii) Example No. 111-121, or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the methods further comprise (after (b)) (c) determining whether a cancer cell in a sample obtained from the subject has the RET inhibitor resistance mutation V804M; and (d) administering a second RET inhibitor, wherein the second RET inhibitor is selected from the group consisting of: N-(1-(5-(3-cyano-6-(2-hydroxy-2-methylpropoxy)pyrazolo[1,5-a]pyridin-4-yl)pyridin-2-yl)-4-methylpiperidin-4-yl)benzamide; 6-ethoxy-4-(6-(4-hydroxy-4-(pyridin-2-ylmethyl)piperidin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-hydroxy-2-methyl propoxy)-4-(6-(3-(pyridin-2-yloxy)azetidin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; 6-(2-hydroxy-2-methylpropoxy)-4-(6-(4-((6-methoxypyridazin-3-yl)oxy)piperidin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; (S)-6-(2-hydroxy-2-methylpropoxy)-4-(6-(3-(pyridin-2-yloxy)pyrrolidin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; N-(1-(5-(3-cyano-6-((3-fluoro-1-methylazetidin-3-yl)methoxy)pyrazolo[1,5-a]pyridin-4-yl)pyridin-2-yl)-4-methylpiperidin-4-yl)-5-fluoro-2-methylbenzamide; 3-chloro-N-(1-(5-(3-cyano-6-((3-fluoro-1-methylazetidin-3-yl)methoxy)pyrazolo[1,5-a]pyridin-4-yl)pyridin-2-yl)-4-methylpiperidin-4-yl)picolinamide; N-((3S,4S)-1-(5-(3-cyano-6-ethoxypyrazolo[1,5-a]pyridin-4-yl)pyridin-2-yl)-3-hydroxypiperidin-4-yl)-3-methylbutanamide; 6-(2-hydroxy-2-methylpropoxy)-4-(6-(4-hydroxy-4-(pyridin-2-ylmethyl)piperidin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile; and 3-chloro-N-((3S,4S)-1-(5-(3-cyano-6-ethoxypyrazolo[1,5-a]pyridin-4-yl)pyrazin-2-yl)-3-hydroxypiperidin-4-yl)picolinamide; or a pharmaceutically acceptable salt or solvate thereof, as a monotherapy or in conjunction with another anticancer agent to the subject if the subject has a cancer cell that has at least one RET inhibitor resistance mutation; or (e) administering additional doses of the compound of Formula I or a pharmaceutically acceptable salt or solvate thereof of step (b) to the subject if the subject has a cancer cell that does not have a RET inhibitor resistance mutation.

In some embodiments, the presence of one or more RET inhibitor resistance mutations in a tumor causes the tumor to be more resistant to treatment with a multikinase inhibitor. Methods useful when a RET inhibitor resistance mutation causes the tumor to be more resistant to treatment with a multikinase inhibitor are described below. For example, provided herein are methods of treating a subject having a cancer that include: identifying a subject having a cancer cell that has one or more RET inhibitor resistance mutations; and administering to the identified subject a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the compound of Formula I or a pharmaceutically acceptable salt or solvate thereof is administered in combination with the multikinase inhibitor. Also provided are methods of treating a subject identified as having a cancer cell that has one or more RET inhibitor resistance mutations that include administering to the subject a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the compound of Formula I or a pharmaceutically acceptable salt or solvate thereof is administered in combination with the multikinase inhibitor. In some embodiments, the one or more RET inhibitor resistance mutations confer increased resistance to a cancer cell or tumor to treatment with the multikinase inhibitor. In some embodiments, the one or more RET inhibitor resistance mutations include one or more RET inhibitor resistance mutations listed in Tables 3 and 4. For example, the one or more RET inhibitor resistance mutations can include a substitution at amino acid position 804, e.g., V804M, V804L, or V804E.

For example, provided herein are methods for treating a RET-associated cancer in a subject in need of such treatment, the method comprising (a) detecting a dysregulation of a RET gene, a RET kinase, or the expression or activity or level of any of the same in a sample from the subject; and (b) administering to the subject a therapeutically effective amount of a multikinase inhibitor, wherein the multikinase inhibitor is selected from vandetanib or cabozantinib; or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the methods further comprise (after (b)) (c) determining whether a cancer cell in a sample obtained from the subject has at least one RET inhibitor resistance mutation; and (d) administering a compound of Formula I, or a pharmaceutically acceptable salt or solvate thereof as a monotherapy or in conjunction with another anticancer agent to the subject if the subject has a cancer cell that has at least one RET inhibitor resistance mutation; or (e) administering additional doses of the multikinase inhibitor of step (b) to the subject if the subject has a cancer cell that does not have a RET inhibitor resistance mutation.

In some embodiments, provided herein are methods for treating a RET-associated cancer in a subject in need of such treatment, the method comprising (a) detecting a dysregulation of a RET gene, a RET kinase, or the expression or activity or level of any of the same in a sample from the subject; and (b) administering to the subject a therapeutically effective amount of a first multikinase inhibitor, wherein the multikinase inhibitor is selected from the group consisting of: vandetanib or cabozantinib; or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the methods further comprise (after (b)) (c) determining whether a cancer cell in a sample obtained from the subject has at least one RET inhibitor resistance mutation; and (d) administering a compound of Formula I selected from i) Example No. 1-20; ii) Example No. 21-40; iii) Example No. 41-49; iv) Example No. 50-70; v) Example No. 71-90; vi) Example No. 91-110; vii) Example No. 111-121, or a pharmaceutically acceptable salt or solvate thereof as a monotherapy or in conjunction with another anticancer agent to the subject if the subject has a cancer cell that has at least one RET inhibitor resistance mutation; or (e) administering additional doses of the multikinase inhibitor of step (b) to the subject if the subject has a cancer cell that does not have a RET inhibitor resistance mutation.

In some embodiments, provided herein are methods for treating a RET-associated cancer in a subject in need of such treatment, the method comprising (a) detecting one or more fusion proteins of Table 1 and/or one or more RET kinase protein point mutations/insertions/deletions of Tables 2 and 2a in a sample from the subject; and (b) administering to the subject a therapeutically effective amount of a multikinase inhibitor, wherein the multikinase inhibitor is selected from the group consisting of: vandetanib or cabozantinib; or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the methods further comprise (after (b)) (c) determining whether a cancer cell in a sample obtained from the subject has at least one RET inhibitor resistance mutation of Tables 3 or 4; and (d) administering a compound of Formula I selected from i) Example No. 1-20; ii) Example No. 21-40; iii) Example No. 41-49; iv) Example No. 50-70; v) Example No. 71-90; vi) Example No. 91-110; vii) Example No. 111-121, or a pharmaceutically acceptable salt or solvate thereof as a monotherapy or in conjunction with another anticancer agent to the subject if the subject has a cancer cell that has at least one RET inhibitor resistance mutation; or (e) administering additional doses of the multikinase inhibitor of step (b) to the subject if the subject has a cancer cell that does not have a RET inhibitor resistance mutation.

In some embodiments, provided herein are methods for treating a RET-associated cancer in a subject in need of such treatment, the method comprising (a) detecting the fusion protein KIF5B-RET in a sample from the subject; and (b) administering to the subject a therapeutically effective amount of a multikinase inhibitor, wherein the multikinase inhibitor is selected from the group consisting of vandetanib or cabozantinib; or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the methods further comprise (after (b)) (c) determining whether a cancer cell in a sample obtained from the subject has the RET inhibitor resistance mutation V804M; and (d) administering a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof selected from the group consisting of a compound of Formula I selected from i) Example No. 1-20; ii) Example No. 21-40; iii) Example No. 41-49; iv) Example No. 50-70; v) Example No. 71-90; vi) Example No. 91-110; vii) Example No. 111-121, or a pharmaceutically acceptable salt or solvate thereof as a monotherapy or in conjunction with another anticancer agent to the subject if the subject has a cancer cell that has at least one RET inhibitor resistance mutation; or (e) administering additional doses of the multikinase inhibitor of step (b) to the subject if the subject has a cancer cell that does not have a RET inhibitor resistance mutation.

As another example, provided herein are methods for treating a RET-associated cancer in a subject in need of such treatment, the method comprising (a) detecting a dysregulation of a RET gene, a RET kinase, or the expression or activity or level of any of the same in a sample from the subject; and (b) administering to the subject a therapeutically effective amount of a compound of Formula I, or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the methods further comprise (after (b)) (c) determining whether a cancer cell in a sample obtained from the subject has at least one RET inhibitor resistance mutation; and (d) administering a multikinase inhibitor (e.g., vandetanib or cabozantinib, as a monotherapy or in conjunction with another anticancer agent to the subject if the subject has a cancer cell that has at least one RET inhibitor resistance mutation; or (e) administering additional doses of the compound of Formula I or a pharmaceutically acceptable salt or solvate thereof of step (b) to the subject if the subject has a cancer cell that does not have a RET inhibitor resistance mutation. In some embodiments, provided herein are methods for treating a RET-associated cancer in a subject in need of such treatment, the method comprising (a) detecting a dysregulation of a RET gene, a RET kinase, or the expression or activity or level of any of the same in a sample from the subject; and (b) administering to the subject a therapeutically effective amount of a compound of Formula I selected from i) Example No. 1-20; ii) Example No. 21-40; iii) Example No. 41-49; iv) Example No. 50-70; v) Example No. 71-90; vi) Example No. 91-110; vii) Example No. 111-121, or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the methods further comprise (after (b)) (c) determining whether a cancer cell in a sample obtained from the subject has at least one RET inhibitor resistance mutation; and (d) administering a multikinase inhibitor (e.g., vandetanib or cabozantinib), as a monotherapy or in conjunction with another anticancer agent to the subject if the subject has a cancer cell that has at least one RET inhibitor resistance mutation; or (e) administering additional doses of the compound of Formula I or a pharmaceutically acceptable salt or solvate thereof of step (b) to the subject if the subject has a cancer cell that does not have a RET inhibitor resistance mutation. In some embodiments, provided herein are methods for treating a RET-associated cancer in a subject in need of such treatment, the method comprising (a) detecting one or more fusion proteins of Table 1 and/or one or more RET kinase protein point mutations/insertions/deletions of Tables 2 and 2a in a sample from the subject; and (b) administering to the subject a therapeutically effective amount of a compound of Formula I selected from i) Example No. 1-20; ii) Example No. 21-40; iii) Example No. 41-49; iv) Example No. 50-70; v) Example No. 71-90; vi) Example No. 91-110; vii) Example No. 111-121, or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the methods further comprise (after (b)) (c) determining whether a cancer cell in a sample obtained from the subject has at least one RET inhibitor resistance mutation of Tables 3 or 4; and (d) administering a multikinase inhibitor (e.g., vandetanib or cabozantinib), as a monotherapy or in conjunction with another anticancer agent to the subject if the subject has a cancer cell that has at least one RET inhibitor resistance mutation; or (e) administering additional doses of the compound of Formula I or a pharmaceutically acceptable salt or solvate thereof of step (b) to the subject if the subject has a cancer cell that does not have a RET inhibitor resistance mutation. In some embodiments, provided herein are methods for treating a RET-associated cancer in a subject in need of such treatment, the method comprising (a) detecting the fusion protein KIF5B-RET in a sample from the subject; and (b) administering to the subject a therapeutically effective amount of a compound of Formula I selected from i) Example No. 1-20; ii) Example No. 21-40; iii) Example No. 41-49; iv) Example No. 50-70; v) Example No. 71-90; vi) Example No. 91-110; vii) Example No. 111-121, or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the methods further comprise (after (b)) (c) determining whether a cancer cell in a sample obtained from the subject has the RET inhibitor resistance mutation V804M; and (d) administering a multikinase inhibitor (e.g., vandetanib or cabozantinib) as a monotherapy or in conjunction with another anticancer agent to the subject if the subject has a cancer cell that has at least one RET inhibitor resistance mutation; or (e) administering additional doses of the compound of Formula I or a pharmaceutically acceptable salt or solvate thereof of step (b) to the subject if the subject has a cancer cell that does not have a RET inhibitor resistance mutation.

Also, provided herein are methods for treating a RET-associated cancer in a subject in need of such treatment, the method comprising (a) detecting a dysregulation of a RET gene, a RET kinase, or the expression or activity or level of any of the same in a sample from the subject; and (b) administering to the subject a therapeutically effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the methods further comprise (after (b)) (c) determining whether a cancer cell in a sample obtained from the subject has at least one RET inhibitor resistance mutation; and (d) administering additional doses of the compound of Formula I or a pharmaceutically acceptable salt or solvate thereof of step (b) to the subject as a monotherapy or in conjunction with another anticancer agent (e.g., a second RET inhibitor, a second compound of Formula I or a pharmaceutically acceptable salt thereof, or immunotherapy) or anticancer therapy (e.g., surgery or radiation) if the subject has a cancer cell that has at least one RET inhibitor resistance mutation. In some embodiments, provided herein are methods for treating a RET-associated cancer in a subject in need of such treatment, the method comprising (a) detecting a dysregulation of a RET gene, a RET kinase, or the expression or activity or level of any of the same in a sample from the subject; and (b) administering to the subject a therapeutically effective amount of a compound of Formula I selected from i) Example No. 1-20; ii) Example No. 21-40; iii) Example No. 41-49; iv) Example No. 50-70; v) Example No. 71-90; vi) Example No. 91-110; vii) Example No. 111-121, or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the methods further comprise (after (b)) (c) determining whether a cancer cell in a sample obtained from the subject has at least one RET inhibitor resistance mutation; and (d) administering additional doses of the compound of Formula I or a pharmaceutically acceptable salt or solvate thereof of step (b) to the subject as a monotherapy or in conjunction with another anticancer agent (e.g., a second RET inhibitor, a second compound of Formula I or a pharmaceutically acceptable salt thereof, or immunotherapy) or anticancer therapy (e.g., surgery or radiation) if the subject has a cancer cell that has at least one RET inhibitor resistance mutation. In some embodiments, provided herein are methods for treating a RET-associated cancer in a subject in need of such treatment, the method comprising (a) detecting one or more fusion proteins of Table 1 and/or one or more RET kinase protein point mutations/insertions/deletions of Tables 2 and 2a in a sample from the subject; and (b) administering to the subject a therapeutically effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof selected from the group consisting of a compound of Formula I selected from i) Example No. 1-20; ii) Example No. 21-40; iii) Example No. 41-49; iv) Example No. 50-70; v) Example No. 71-90; vi) Example No. 91-110; vii) Example No. 111-121, or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the methods further comprise (after (b)) (c) determining whether a cancer cell in a sample obtained from the subject has at least one RET inhibitor resistance mutation of Tables 3 or 4; and (d) administering additional doses of the compound of Formula I or a pharmaceutically acceptable salt or solvate thereof of step (b) to the subject as a monotherapy or in conjunction with another anticancer agent (e.g., a second RET inhibitor, a second compound of Formula I or a pharmaceutically acceptable salt thereof, or immunotherapy) or anticancer therapy (e.g., surgery or radiation) if the subject has a cancer cell that has at least one RET inhibitor resistance mutation. In some embodiments, a second RET inhibitor selected from the group consisting of alectinib, cabozantinib, lenvatinib, nintedanib, ponatinib, regorfenib, sorafenib, sunitinib, vandetanib, RXDX-105 (agerafenib), LOXO-292, BLU-667, BLU6864, DS-5010, GSK3179106, GSK3352589, and NMS-E668 is administered in step (d). In some embodiments, provided herein are methods for treating a RET-associated cancer in a subject in need of such treatment, the method comprising (a) detecting the fusion protein KIF5B-RET in a sample from the subject; and (b) administering to the subject a therapeutically effective amount of a compound of Formula I selected from i) Example No. 1-20; ii) Example No. 21-40; iii) Example No. 41-49; iv) Example No. 50-70; v) Example No. 71-90; vi) Example No. 91-110; vii) Example No. 111-121, or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the methods further comprise (after (b)) (c) determining whether a cancer cell in a sample obtained from the subject has the RET inhibitor resistance mutation V804M; and (d) administering additional doses of the compound of Formula I or a pharmaceutically acceptable salt or solvate thereof of step (b) to the subject as a monotherapy or in conjunction with another anticancer agent (e.g., a second RET inhibitor, a second compound of Formula I or a pharmaceutically acceptable salt thereof, or immunotherapy) or anticancer therapy (e.g., surgery or radiation) if the subject has a cancer cell that has at least one RET inhibitor resistance mutation. In some embodiments, a second RET inhibitor selected from the group consisting of alectinib, cabozantinib, lenvatinib, nintedanib, ponatinib, regorfenib, sorafenib, sunitinib, vandetanib, RXDX-105 (agerafenib), LOXO-292, BLU-667, BLU6864, DS-5010, GSK3179106, GSK3352589, and NMS-E668 is administered in step (d).

Also, provided herein are methods for treating a RET-associated cancer in a subject in need of such treatment, the method comprising (a) detecting a dysregulation of a RET gene, a RET kinase, or the expression or activity or level of any of the same in a sample from the subject; and (b) administering to the subject a therapeutically effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the methods further comprise (after (b)) (c) detecting at least one RET inhibitor resistance mutation in a cancer cell in a sample obtained from the subject; and (d) administering additional doses of the compound of Formula I or a pharmaceutically acceptable salt or solvate thereof of step (b) to the subject as a monotherapy or in conjunction with another anticancer agent (e.g., a second RET inhibitor, a second compound of Formula I or a pharmaceutically acceptable salt thereof, or immunotherapy) or anticancer therapy (e.g., surgery or radiation). In some embodiments, provided herein are methods for treating a RET-associated cancer in a subject in need of such treatment, the method comprising (a) detecting a dysregulation of a RET gene, a RET kinase, or the expression or activity or level of any of the same in a sample from the subject; and (b) administering to the subject a therapeutically effective amount of a compound of Formula I selected from i) Example No. 1-20; ii) Example No. 21-40; iii) Example No. 41-49; iv) Example No. 50-70; v) Example No. 71-90; vi) Example No. 91-110; vii) Example No. 111-121, or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the methods further comprise (after (b)) (c) detecting at least one RET inhibitor resistance mutation in a cancer cell in a sample obtained from the subject; and (d) administering additional doses of the compound of Formula I or a pharmaceutically acceptable salt or solvate thereof of step (b) to the subject as a monotherapy or in conjunction with another anticancer agent (e.g., a second RET inhibitor, a second compound of Formula I or a pharmaceutically acceptable salt thereof, or immunotherapy) or anticancer therapy (e.g., surgery or radiation). In some embodiments, provided herein are methods for treating a RET-associated cancer in a subject in need of such treatment, the method comprising (a) detecting one or more fusion proteins of Table 1 and/or one or more RET kinase protein point mutations/insertions/deletions of Tables 2 and 2a in a sample from the subject; and (b) administering to the subject a therapeutically effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof selected from the group consisting of a compound of Formula I selected from i) Example No. 1-20; ii) Example No. 21-40; iii) Example No. 41-49; iv) Example No. 50-70; v) Example No. 71-90; vi) Example No. 91-110; vii) Example No. 111-121, or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the methods further comprise (after (b)) (c) detecting at least one RET inhibitor resistance mutation of Tables 3 or 4 in a cancer cell in a sample obtained from the subject; and (d) administering additional doses of the compound of Formula I or a pharmaceutically acceptable salt or solvate thereof of step (b) to the subject as a monotherapy or in conjunction with another anticancer agent (e.g., a second RET inhibitor, a second compound of Formula I or a pharmaceutically acceptable salt thereof, or immunotherapy) or anticancer therapy (e.g., surgery or radiation). In some embodiments, a second RET inhibitor selected from the group consisting of alectinib, cabozantinib, lenvatinib, nintedanib, ponatinib, regorfenib, sorafenib, sunitinib, vandetanib, RXDX-105 (agerafenib), LOXO-292, BLU-667, BLU6864, DS-5010, GSK3179106, GSK3352589, and NMS-E668 is administered in step (d). In some embodiments, provided herein are methods for treating a RET-associated cancer in a subject in need of such treatment, the method comprising (a) detecting the fusion protein KIF5B-RET in a sample from the subject; and (b) administering to the subject a therapeutically effective amount of a compound of Formula I selected from i) Example No. 1-20; ii) Example No. 21-40; iii) Example No. 41-49; iv) Example No. 50-70; v) Example No. 71-90; vi) Example No. 91-110; vii) Example No. 111-121, or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the methods further comprise (after (b)) (c) detecting the RET inhibitor resistance mutation V804M in a cancer cell in a sample obtained from the subject; and (d) administering additional doses of the compound of Formula I or a pharmaceutically acceptable salt or solvate thereof of step (b) to the subject as a monotherapy or in conjunction with another anticancer agent (e.g., a second RET inhibitor, a second compound of Formula I or a pharmaceutically acceptable salt thereof, or immunotherapy) or anticancer therapy (e.g., surgery or radiation). In some embodiments, a second RET inhibitor selected from the group consisting of alectinib, cabozantinib, lenvatinib, nintedanib, ponatinib, regorfenib, sorafenib, sunitinib, vandetanib, RXDX-105 (agerafenib), LOXO-292, BLU-667, BLU6864, DS-5010, GSK3179106, GSK3352589, and NMS-E668 is administered in step (d).

Also provided are methods of selecting a treatment for a subject having a cancer that include: identifying a subject having a cancer cell that has one or more RET inhibitor resistance mutations; and selecting a treatment that includes administration of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the one or more RET inhibitor resistance mutations confer increased resistance to a cancer cell or tumor to treatment with a first RET inhibitor. In some embodiments, the compound of Formula I or a pharmaceutically acceptable salt or solvate thereof is administered in combination with the first RET inhibitor. Also provided are methods of selecting a treatment for a subject having a cancer that include: selecting a treatment that includes administration of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof for a subject identified as having a cancer cell that has one or more RET inhibitor resistance mutations. Also provided are methods of selecting a subject having a cancer for a treatment that does not include a first RET inhibitor as a monotherapy that include: identifying a subject having a cancer cell that has one or more RET inhibitor resistance mutations; and selecting the identified subject for a treatment that includes a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof. Also provided are methods of selecting a subject having a cancer for a treatment that does not include a first RET inhibitor as a monotherapy that include: selecting a subject identified as having a cancer cell that has one or more RET inhibitor resistance mutations for a treatment that includes administration of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the one or more RET inhibitor resistance mutations include one or more RET inhibitor resistance mutations listed in Tables 3 and 4. In some embodiments, the one or more RET inhibitor resistance mutations can include a substitution at amino acid position 804, e.g., V804M, V804L, or V804E.

Also provided are methods of determining the likelihood that a subject having a cancer (e.g., a RET-associated cancer) will have a positive response to treatment with a first RET inhibitor as a monotherapy that include: determining whether a cancer cell in a sample obtained from the subject has one or more RET inhibitor resistance mutations; and determining that a subject having a cancer cell that has one or more RET inhibitor resistance mutations has a decreased likelihood of having a positive response (i.e. an increased likelihood of having a negative response) to treatment with a first RET inhibitor as a monotherapy. Also provided are methods of determining the likelihood that a subject having a cancer (e.g., a RET-associated cancer) will have a positive response to treatment with a first RET inhibitor as a monotherapy that include: determining whether a cancer cell in a sample obtained from the subject has one or more RET inhibitor resistance mutations; and determining that a subject not having a cancer cell that has one or more RET inhibitor resistance mutations has an increased likelihood of having a positive response to treatment with a first RET inhibitor as a monotherapy as compared to a subject having a cancer cell that has one or more RET inhibitor resistance mutations. Also provided are methods of predicting the efficacy of treatment with a first RET inhibitor as a monotherapy in a subject having cancer that include: determining whether a cancer cell in a sample obtained from the subject has one or more RET inhibitor resistance mutations; and determining that treatment with a first RET inhibitor as a monotherapy is less likely to be effective in a subject having a cancer cell in a sample obtained from the subject that has one or more RET inhibitor resistance mutations. Also provided are methods of predicting the efficacy of treatment with a first RET inhibitor as a monotherapy in a subject having cancer that include: determining that treatment with a first RET inhibitor as a monotherapy is less likely to be effective in a subject having a cancer cell in a sample obtained from the subject that has one or more RET inhibitor resistance mutations. In some embodiments, the one or more RET inhibitor resistance mutations confer increased resistance to a cancer cell or tumor to treatment with the first RET inhibitor. In some embodiments, the one or more RET inhibitor resistance mutations include one or more RET inhibitor resistance mutations listed in Tables 3 and 4. For example, the one or more RET inhibitor resistance mutations can include a substitution at amino acid position 804, e.g., V804M, V804L, or V804E.

Also provided are methods of treating a subject having a cancer that include: (a) administering one or more doses of a first RET inhibitor to the subject for a period of time; (b) after (a), determining whether a cancer cell in a sample obtained from the subject has at least one RET inhibitor resistance mutation; and (c) administering a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof as a monotherapy or in conjunction with another anticancer agent to the subject if the subject has a cancer cell that has at least one RET inhibitor resistance mutation; or (d) administering additional doses of the first RET inhibitor of step (a) to the subject if the subject has a cancer cell that does not have a RET inhibitor resistance mutation. In some embodiments, where the subject is administered additional doses of the first RET inhibitor of step (a), the subject can also be administered another anticancer agent (e.g., a second RET inhibitor or a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof, or immunotherapy). In some embodiments, the additional anticancer agent is any anticancer agent known in the art. For example, the additional anticancer agent is another RET inhibitor (e.g., a second RET inhibitor). In some embodiments, the additional anticancer agent is an immunotherapy. In some embodiments of step (c), another RET inhibitor can be the first RET inhibitor administered in step (a). In some embodiments, the one or more RET inhibitor resistance mutations confer increased resistance to a cancer cell or tumor to treatment with the first RET inhibitor. In some embodiments, the one or more RET inhibitor resistance mutations include one or more RET inhibitor resistance mutations listed in Tables 3 and 4. For example, the one or more RET inhibitor resistance mutations can include a substitution at amino acid position 804, e.g., V804M, V804L, or V804E.

Also provided are methods of treating a subject having a cancer that include: (a) administering one or more doses of a first RET inhibitor to the subject for a period of time; (b) after (a), determining whether a cancer cell in a sample obtained from the subject has at least one RET inhibitor resistance mutation; and (c) administering a second RET inhibitor as a monotherapy or in conjunction with another anticancer agent to the subject if the subject has a cancer cell that has at least one RET inhibitor resistance mutation; or (d) administering additional doses of the first RET inhibitor step (a) to the subject if the subject has a cancer cell that does not have a RET inhibitor resistance mutation. In some embodiments, where the subject is administered additional doses of the first RET inhibitor of step (a), the subject can also be administered another anticancer agent. In some embodiments, the one or more RET inhibitor resistance mutations confer increased resistance to a cancer cell or tumor to treatment with the first RET inhibitor. In some embodiments, the one or more RET inhibitor resistance mutations include one or more RET inhibitor resistance mutations listed in Tables 3 and 4. For example, the one or more RET inhibitor resistance mutations can include a substitution at amino acid position 804, e.g., V804M, V804L, or V804E. In some embodiments, the additional anticancer agent is any anticancer agent known in the art. For example, the additional anticancer agent is another RET inhibitor (e.g., a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof). In some embodiments, the additional anticancer agent is an immunotherapy.

Also provided are methods of treating a subject having a cancer (e.g., a RET-associated cancer) that include: (a) determining whether a cancer cell in a sample obtained from a subject having a cancer and previously administered one or more doses of a first RET inhibitor, has one or more RET inhibitor resistance mutations; and (b) administering a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof as a monotherapy or in conjunction with another anticancer agent to the subject if the subject has a cancer cell that has at least one RET inhibitor resistance mutation; or (c) administering additional doses of the first RET inhibitor previously administered to the subject if the subject has cancer cell that does not have a RET inhibitor resistance mutation. In some embodiments, where the subject is administered additional doses of the first RET inhibitor previously administered to the subject, the subject can also be administered another anticancer agent (e.g., a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof, or immunotherapy). In some embodiments, the one or more RET inhibitor resistance mutations confer increased resistance to a cancer cell or tumor to treatment with the first RET inhibitor. In some embodiments, the one or more RET inhibitor resistance mutations include one or more RET inhibitor resistance mutations listed in Tables 3 and 4. For example, the one or more RET inhibitor resistance mutations can include a substitution at amino acid position 804, e.g., V804M, V804L, or V804E. In some embodiments, the additional anticancer agent is any anticancer agent known in the art. For example, the additional anticancer agent is another RET inhibitor (e.g., a second RET inhibitor). In some embodiments, the additional anticancer agent is an immunotherapy. In some embodiments of step (b), another anticancer agent can be the first RET inhibitor administered in step (a).

Also provided are methods of treating a subject having a cancer that include: (a) determining whether a cancer cell in a sample obtained from a subject having a cancer and previously administered one or more doses of a first RET inhibitor has one or more RET inhibitor resistance mutations; and (b) administering a second RET inhibitor as a monotherapy or in conjunction with another anticancer agent to the subject if the subject has a cancer cell that has at least one RET inhibitor resistance mutation; or (c) administering additional doses of the first RET inhibitor previously administered to the subject if the subject has a cancer cell that does not have a RET inhibitor resistance mutation. In some embodiments, where the subject is administered additional doses of the first RET inhibitor previously administered to the subject, the subject can also be administered another anticancer agent. In some embodiments, the one or more RET inhibitor resistance mutations confer increased resistance to a cancer cell or tumor to treatment with the first RET inhibitor. In some embodiments, the one or more RET inhibitor resistance mutations include one or more RET inhibitor resistance mutations listed in Tables 3 and 4. For example, the one or more RET inhibitor resistance mutations can include a substitution at amino acid position 804, e.g., V804M, V804L, or V804E. In some embodiments, the additional anticancer agent is any anticancer agent known in the art. For example, the additional anticancer agent is another RET inhibitor (e.g., a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof). In some embodiments, the additional anticancer agent is an immunotherapy. In some embodiments of (b), another anticancer agent can be the first RET inhibitor administered in step (a).

Treatment of a patient having a cancer with a multi-kinase inhibitor (MKI) or target-specific kinase inhibitor (e.g., a BRAF inhibitor, a EGFR inhibitor, a MEK inhibitor, an ALK inhibitor, a ROS1 inhibitor, a MET inhibitor, an aromatase inhibitor, a RAF inhibitor, or a RAS inhibitor) can result in dysregulation of a RET gene, a RET kinase, or the expression or activity or level of the same in the cancer, and/or resistance to a RET inhibitor. See, e.g., Bhinge et al., Oncotarget 8:27155-27165, 2017; Chang et al., Yonsei Med. J. 58:9-18, 2017; and Lopez-Delisle et al., doi: 10.1038/s41388-017-0039-5, Oncogene 2018.

Treatment of a patient having a cancer with a RET inhibitor in combination with a multi-kinase inhibitor or a target-specific kinase inhibitor (e.g., a BRAF inhibitor, a EGFR inhibitor, a MEK inhibitor, an ALK inhibitor, a ROS1 inhibitor, a MET inhibitor, an aromatase inhibitor, a RAF inhibitor, or a RAS inhibitor) can have increased therapeutic efficacy as compared to treatment of the same patient or a similar patient with the RET inhibitor as a monotherapy, or the multi-kinase inhibitor or the target-specific kinase inhibitor as a monotherapy. See, e.g., Tang et al., doi: 10.1038/modpathol.2017.109, Mod. Pathol. 2017; Andreucci et al., Oncotarget 7:80543-80553, 2017; Nelson-Taylor et al., Mol. Cancer Ther. 16:1623-1633, 2017; and Kato et al., Clin. Cancer Res. 23:1988-1997, 2017.

Provided herein are methods of treating a patient having a cancer (e.g., any of the cancers described herein) and previously administered a multi-kinase inhibitor (MKI) or a target-specific kinase inhibitor (e.g., a BRAF inhibitor, a EGFR inhibitor, a MEK inhibitor, an ALK inhibitor, a ROS1 inhibitor, a MET inhibitor, an aromatase inhibitor, a RAF inhibitor, or a RAS inhibitor) (e.g., as a monotherapy) that include: administering to the patient (i) a therapeutically effective dose of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof as a monotherapy, or (ii) a therapeutically effective dose of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof, and a therapeutically effective dose of the previously administered MKI or the previously administered target-specific kinase inhibitor.

Provided herein are methods of treating a patient having a cancer (e.g., any of the cancers described herein) previously administered a MKI or a target specific kinase inhibitor (e.g., a BRAF inhibitor, a EGFR inhibitor, a MEK inhibitor, an ALK inhibitor, a ROS1 inhibitor, a MET inhibitor, an aromatase inhibitor, a RAF inhibitor, or a RAS inhibitor) (e.g., as a monotherapy) that include: identifying a patient having a cancer cell that has a dysregulation of a RET gene, a RET kinase, or the expression or activity or level of the same; and administering to the identified patient (i) a therapeutically effective dose of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof as a monotherapy, or (ii) a therapeutically effective dose of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof, and a therapeutically effective dose of the previously administered MKI or the previously administered target-specific kinase inhibitor.

Provided herein are methods of treating a patient having a cancer (e.g., any of the cancers described herein) that include: administering to a patient a therapeutically effective amount of a MKI or a target-specific kinase inhibitor (e.g., a BRAF inhibitor, a EGFR inhibitor, a MEK inhibitor, an ALK inhibitor, a ROS1 inhibitor, a MET inhibitor, an aromatase inhibitor, a RAF inhibitor, or a RAS inhibitor) (e.g., as a monotherapy) for a first period of time; after the period of time, identifying a patient having a cancer cell that has a dysregulation of a RET gene, a RET kinase, or the expression or activity or level of the same; and administering to the identified patient (i) a therapeutically effective dose of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof as a monotherapy, or (ii) a therapeutically effective dose of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof, and a therapeutically effective dose of the previously administered MKI or the previously administered target-specific kinase inhibitor.

Provided herein are methods of treating a patient having a cancer (e.g., any of the cancers described herein) that has dysregulation of a BRAF gene, a BRAF kinase, or the expression or activity or level of the same that include administering to the patient (i) a therapeutically effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof and (ii) a therapeutically effective amount of a BRAF inhibitor (e.g., any of the BRAF inhibitors described herein or known in the art).

Provided herein are methods of treating a patient having a cancer (e.g., any of the cancers described herein) that include: identifying a patient having a cancer cell that has dysregulation of a BRAF gene, a BRAF kinase, or the expression or activity or level of the same; and administering to the identified patient (i) a therapeutically effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof and (ii) a therapeutically effective amount of a BRAF inhibitor (e.g., any of the BRAF inhibitors described herein or known in the art).

Provided herein are methods of treating a patient having a cancer (e.g., any of the cancers described herein) that has dysregulation of an EGFR gene, an EGFR protein, or the expression or activity or level of the same that include administering to the patient (i) a therapeutically effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof and (ii) a therapeutically effective amount of an EGFR inhibitor (e.g., any of the EGFR inhibitors described herein or known in the art).

Provided herein are methods of treating a patient having a cancer (e.g., any of the cancers described herein) that include: identifying a patient having a cancer cell that has dysregulation of an EGFR gene, an EGFR protein, or the expression or activity or level of the same; and administering to the identified patient (i) a therapeutically effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof and (ii) a therapeutically effective amount of an EGFR inhibitor (e.g., any of the EGFR inhibitors described herein or known in the art).

Provided herein are methods of treating a patient having a cancer (e.g., any of the cancers described herein) that has dysregulation of a MEK gene, a MEK protein, or the expression or activity or level of the same that include administering to the patient (i) a therapeutically effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof and (ii) a therapeutically effective amount of a MEK inhibitor (e.g., any of the MEK inhibitors described herein or known in the art).

Provided herein are methods of treating a patient having a cancer (e.g., any of the cancers described herein) that include: identifying a patient having a cancer cell that has dysregulation of a MEK gene, a MEK protein, or the expression or activity or level of the same; and administering to the identified patient (i) a therapeutically effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof and (ii) a therapeutically effective amount of a MEK inhibitor (e.g., any of the MEK inhibitors described herein or known in the art).

Provided herein are methods of treating a patient having a cancer (e.g., any of the cancers described herein) that has dysregulation of an ALK gene, an ALK protein, or the expression or activity or level of the same that include administering to the patient (i) a therapeutically effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof and (ii) a therapeutically effective amount of an ALK inhibitor (e.g., any of the ALK inhibitors described herein or known in the art).

Provided herein are methods of treating a patient having a cancer (e.g., any of the cancers described herein) that include: identifying a patient having a cancer cell that has dysregulation of an ALK gene, an ALK protein, or the expression or activity or level of the same; and administering to the identified patient (i) a therapeutically effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof and (ii) a therapeutically effective amount an ALK inhibitor (e.g., any of the ALK inhibitors described herein or known in the art).

Provided herein are methods of treating a patient having a cancer (e.g., any of the cancers described herein) that has dysregulation of a ROS gene, a ROS protein, or the expression or activity or level of the same that include administering to the patient (i) a therapeutically effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof and (ii) a therapeutically effective amount of a ROS inhibitor (e.g., any of the ROS inhibitors described herein or known in the art).

Provided herein are methods of treating a patient having a cancer (e.g., any of the cancers described herein) that include: identifying a patient having a cancer cell that has dysregulation of a ROS gene, a ROS protein, or the expression or activity or level of the same; and administering to the identified patient (i) a therapeutically effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof and (ii) a therapeutically effective amount a ROS inhibitor (e.g., any of the ROS inhibitors described herein or known in the art).

Provided herein are methods of treating a patient having a cancer (e.g., any of the cancers described herein) that has dysregulation of a MET gene, a MET protein, or the expression or activity or level of the same that include administering to the patient (i) a therapeutically effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof and (ii) a therapeutically effective amount of a MET inhibitor (e.g., any of the MET inhibitors described herein or known in the art).

Provided herein are methods of treating a patient having a cancer (e.g., any of the cancers described herein) that include: identifying a patient having a cancer cell that has dysregulation of a MET gene, a MET protein, or the expression or activity or level of the same; and administering to the identified patient (i) a therapeutically effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof and (ii) a therapeutically effective amount a MET inhibitor (e.g., any of the MET inhibitors described herein or known in the art).

Provided herein are methods of treating a patient having a cancer (e.g., any of the cancers described herein) that has dysregulation of an aromatase gene, an aromatase protein, or the expression or activity or level of the same that include administering to the patient (i) a therapeutically effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof and (ii) a therapeutically effective amount of an aromatase inhibitor (e.g., any of the aromatase inhibitors described herein or known in the art).

Provided herein are methods of treating a patient having a cancer (e.g., any of the cancers described herein) that include: identifying a patient having a cancer cell that has dysregulation of an aromatase gene, an aromatase protein, or the expression or activity or level of the same; and administering to the identified patient (i) a therapeutically effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof and (ii) a therapeutically effective amount an aromatase inhibitor (e.g., any of the aromatase inhibitors described herein or known in the art).

Provided herein are methods of treating a patient having a cancer (e.g., any of the cancers described herein) that has dysregulation of a RAF gene, a RAF protein, or the expression or activity or level of the same that include administering to the patient (i) a therapeutically effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof and (ii) a therapeutically effective amount of a RAF inhibitor (e.g., any of the RAF inhibitors described herein or known in the art).

Provided herein are methods of treating a patient having a cancer (e.g., any of the cancers described herein) that include: identifying a patient having a cancer cell that has dysregulation of a RAF gene, a RAF protein, or the expression or activity or level of the same; and administering to the identified patient (i) a therapeutically effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof and (ii) a therapeutically effective amount a RAF inhibitor (e.g., any of the RAF inhibitors described herein or known in the art).

Provided herein are methods of treating a patient having a cancer (e.g., any of the cancers described herein) that has dysregulation of a RAS gene, a RAS protein, or the expression or activity or level of the same that include administering to the patient (i) a therapeutically effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof and (ii) a therapeutically effective amount of a RAS inhibitor (e.g., any of the RAS inhibitors described herein or known in the art).

Provided herein are methods of treating a patient having a cancer (e.g., any of the cancers described herein) that include: identifying a patient having a cancer cell that has dysregulation of a RAS gene, a RAS protein, or the expression or activity or level of the same; and administering to the identified patient (i) a therapeutically effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof and (ii) a therapeutically effective amount a RAS inhibitor (e.g., any of the RAS inhibitors described herein or known in the art).

The phrase “dysregulation of a BRAF gene, a BRAF protein, or the expression or activity or level of any of the same” refers to a genetic mutation (e.g., a chromosomal translocation that results in the expression of a fusion protein including a BRAF kinase domain and a fusion partner, a mutation in a BRAF gene that results in the expression of a BRAF protein that includes a deletion of at least one amino acid as compared to a wildtype BRAF protein, a mutation in a BRAF gene that results in the expression of a BRAF protein with one or more point mutations as compared to a wildtype BRAF protein, a mutation in a BRAF gene that results in the expression of a BRAF protein with at least one inserted amino acid as compared to a wildtype BRAF protein, a gene duplication that results in an increased level of BRAF protein in a cell, or a mutation in a regulatory sequence (e.g., a promoter and/or enhancer) that results in an increased level of BRAF protein in a cell), an alternative spliced version of a BRAF mRNA that results in a BRAF protein having a deletion of at least one amino acid in the BRAF protein as compared to the wild-type BRAF protein), or increased expression (e.g., increased levels) of a wildtype BRAF protein in a mammalian cell due to aberrant cell signaling and/or dysregulated autocrine/paracrine signaling (e.g., as compared to a control non-cancerous cell). As another example, a dysregulation of a BRAF gene, a BRAF protein, or expression or activity, or level of any of the same, can be a mutation in a BRAF gene that encodes a BRAF protein that is constitutively active or has increased activity as compared to a protein encoded by a BRAF gene that does not include the mutation. For example, a dysregulation of a BRAF gene, a BRAF protein, or expression or activity, or level of any of the same, can be the result of a gene or chromosome translocation which results in the expression of a fusion protein that contains a first portion of a BRAF protein that includes a functional kinase domain, and a second portion of a partner protein (i.e., that is not BRAF). In some examples, dysregulation of a BRAF gene, a BRAF protein, or expression or activity or level of any of the same can be a result of a gene translocation of one BRAF gene with another non-BRAF gene.

Non-limiting examples of a BRAF inhibitor include dabrafenib, vemurafenib (also called RG7204 or PLX4032), sorafenib tosylate, PLX-4720, GDC-0879, BMS-908662 (Bristol-Meyers Squibb), LGX818 (Novartis), PLX3603 (Hofmann-LaRoche), RAF265 (Novartis), R05185426 (Hofmann-LaRoche), and GSK2118436 (GlaxoSmithKline). Additional examples of a BRAF inhibitor are known in the art.

The phrase “dysregulation of an EGFR gene, an EGFR protein, or the expression or activity or level of any of the same” refers to a genetic mutation (e.g., a chromosomal translocation that results in the expression of a fusion protein including an EGFR kinase domain and a fusion partner, a mutation in an EGFR gene that results in the expression of an EGFR protein that includes a deletion of at least one amino acid as compared to a wildtype EGFR protein, a mutation in an EGFR gene that results in the expression of an EGFR protein with one or more point mutations as compared to a wildtype EGFR protein, a mutation in an EGFR gene that results in the expression of an EGFR protein with at least one inserted amino acid as compared to a wildtype EGFR protein, a gene duplication that results in an increased level of EGFR protein in a cell, or a mutation in a regulatory sequence (e.g., a promoter and/or enhancer) that results in an increased level of EGFR protein in a cell), an alternative spliced version of a EGFR mRNA that results in an EGFR protein having a deletion of at least one amino acid in the EGFR protein as compared to the wild-type EGFR protein), or increased expression (e.g., increased levels) of a wildtype EGFR protein in a mammalian cell due to aberrant cell signaling and/or dysregulated autocrine/paracrine signaling (e.g., as compared to a control non-cancerous cell). As another example, a dysregulation of an EGFR gene, an EGFR protein, or expression or activity, or level of any of the same, can be a mutation in an EGFR gene that encodes an EGFR protein that is constitutively active or has increased activity as compared to a protein encoded by an EGFR gene that does not include the mutation. For example, a dysregulation of an EGFR gene, an EGFR protein, or expression or activity, or level of any of the same, can be the result of a gene or chromosome translocation which results in the expression of a fusion protein that contains a first portion of a EGFR protein that includes a functional kinase domain, and a second portion of a partner protein (i.e., that is not EGFR). In some examples, dysregulation of an EGFR gene, an EGFR protein, or expression or activity or level of any of the same can be a result of a gene translocation of one EGFR gene with another non-EGFR gene.

Non-limiting examples of an EGFR inhibitor include gefitinib, erlotinib, brigatinib, lapatinib, neratinib, icotinib, afatinib, dacomitinib, poziotinib, vandetanib, afatinib, AZD9291, CO-1686, HM61713, AP26113, CI-1033, PKI-166, GW-2016, EKB-569, PDI-168393, AG-1478, CGP-59326A. Additional examples of an EGFR inhibitor are known in the art.

The phrase “dysregulation of a MEK gene, a MEK protein, or the expression or activity or level of any of the same” refers to a genetic mutation (e.g., a chromosomal translocation that results in the expression of a fusion protein including a MEK kinase domain and a fusion partner, a mutation in a MEK gene that results in the expression of a MEK protein that includes a deletion of at least one amino acid as compared to a wildtype MEK protein, a mutation in a MEK gene that results in the expression of a MEK protein with one or more point mutations as compared to a wildtype MEK protein, a mutation in a MEK gene that results in the expression of a MEK protein with at least one inserted amino acid as compared to a wildtype MEK protein, a gene duplication that results in an increased level of MEK protein in a cell, or a mutation in a regulatory sequence (e.g., a promoter and/or enhancer) that results in an increased level of MEK protein in a cell), an alternative spliced version of a MEK mRNA that results in a MEK protein having a deletion of at least one amino acid in the MEK protein as compared to the wild-type MEK protein), or increased expression (e.g., increased levels) of a wildtype MEK protein in a mammalian cell due to aberrant cell signaling and/or dysregulated autocrine/paracrine signaling (e.g., as compared to a control non-cancerous cell). As another example, a dysregulation of a MEK gene, a MEK protein, or expression or activity, or level of any of the same, can be a mutation in a MEK gene that encodes a MEK protein that is constitutively active or has increased activity as compared to a protein encoded by a MEK gene that does not include the mutation. For example, a dysregulation of a MEK gene, a MEK protein, or expression or activity, or level of any of the same, can be the result of a gene or chromosome translocation which results in the expression of a fusion protein that contains a first portion of a MEK protein that includes a functional kinase domain, and a second portion of a partner protein (i.e., that is not MEK). In some examples, dysregulation of a MEK gene, a MEK protein, or expression or activity or level of any of the same can be a result of a gene translocation of one MEK gene with another non-MEK gene.

Non-limiting examples of a MEK inhibitor include mekinist, trametinib (GSK1120212), cobimetinib (XL518), binimetinib (MEK162), selumetinib, PD-325901, CI-1040, PD035901, TAK-733, PD098059, U0126, AS703026/MSC1935369, XL-518/GDC-0973, BAY869766/RDEA119, and GSK1120212. Additional examples of a MEK inhibitor are known in the art.

The phrase “dysregulation of an ALK gene, an ALK protein, or the expression or activity or level of any of the same” refers to a genetic mutation (e.g., a chromosomal translocation that results in the expression of a fusion protein including an ALK kinase domain and a fusion partner, a mutation in an ALK gene that results in the expression an ALK protein that includes a deletion of at least one amino acid as compared to a wildtype ALK protein, a mutation in an ALK gene that results in the expression of an ALK protein with one or more point mutations as compared to a wildtype ALK protein, a mutation in an ALK gene that results in the expression of an ALK protein with at least one inserted amino acid as compared to a wildtype ALK protein, a gene duplication that results in an increased level of ALK protein in a cell, or a mutation in a regulatory sequence (e.g., a promoter and/or enhancer) that results in an increased level of ALK protein in a cell), an alternative spliced version of an ALK mRNA that results in an ALK protein having a deletion of at least one amino acid in the ALK protein as compared to the wild-type ALK protein), or increased expression (e.g., increased levels) of a wildtype ALK protein in a mammalian cell due to aberrant cell signaling and/or dysregulated autocrine/paracrine signaling (e.g., as compared to a control non-cancerous cell). As another example, a dysregulation of an ALK gene, an ALK protein, or expression or activity, or level of any of the same, can be a mutation in an ALK gene that encodes an ALK protein that is constitutively active or has increased activity as compared to a protein encoded by an ALK gene that does not include the mutation. For example, a dysregulation of an ALK gene, an ALK protein, or expression or activity, or level of any of the same, can be the result of a gene or chromosome translocation which results in the expression of a fusion protein that contains a first portion of an ALK protein that includes a functional kinase domain, and a second portion of a partner protein (i.e., that is not ALK). In some examples, dysregulation of an ALK gene, an ALK protein, or expression or activity or level of any of the same can be a result of a gene translocation of one ALK gene with another non-ALK gene.

Non-limiting examples of an ALK inhibitor include crizotinib (Xalkori), ceritinib (Zykadia), alectinib (Alecensa), dalantercept, ACE-041 (Brigatinib) (AP26113), entrectinib (NMS-E628), PF-06463922 (Pfizer), TSR-011 (Tesaro), CEP-37440 (Teva), CEP-37440 (Teva), X-396 (Xcovery), and ASP-3026 (Astellas). Additional examples of an ALK inhibitor are known in the art.

The phrase “dysregulation of a ROS1 gene, a ROS1 protein, or the expression or activity or level of any of the same” refers to a genetic mutation (e.g., a chromosomal translocation that results in the expression of a fusion protein including a ROS1 kinase domain and a fusion partner, a mutation in a ROS1 gene that results in the expression a ROS1 protein that includes a deletion of at least one amino acid as compared to a wildtype ROS1 protein, a mutation in a ROS1 gene that results in the expression of a ROS1 protein with one or more point mutations as compared to a wildtype ROS1 protein, a mutation in a ROS1 gene that results in the expression of a ROS1 protein with at least one inserted amino acid as compared to a wildtype ROS1 protein, a gene duplication that results in an increased level of ROS1 protein in a cell, or a mutation in a regulatory sequence (e.g., a promoter and/or enhancer) that results in an increased level of ROS1 protein in a cell), an alternative spliced version of a ROS1 mRNA that results in a ROS1 protein having a deletion of at least one amino acid in the ROS1 protein as compared to the wild-type ROS1 protein), or increased expression (e.g., increased levels) of a wildtype ROS1 protein in a mammalian cell due to aberrant cell signaling and/or dysregulated autocrine/paracrine signaling (e.g., as compared to a control non-cancerous cell). As another example, a dysregulation of a ROS1 gene, a ROS1 protein, or expression or activity, or level of any of the same, can be a mutation in a ROS1 gene that encodes a ROS1 protein that is constitutively active or has increased activity as compared to a protein encoded by a ROS1 gene that does not include the mutation. For example, a dysregulation of a ROS1 gene, a ROS1 protein, or expression or activity, or level of any of the same, can be the result of a gene or chromosome translocation which results in the expression of a fusion protein that contains a first portion of a ROS1 protein that includes a functional kinase domain, and a second portion of a partner protein (i.e., that is not ROS1). In some examples, dysregulation of a ROS1 gene, a ROS1 protein, or expression or activity or level of any of the same can be a result of a gene translocation of one ROS1 gene with another non-ROS1 gene.

Non-limiting examples of a ROS1 inhibitor include crizotinib, entrectinib (RXDX-101), lorlatinib (PF-06463922), certinib, TPX-0005, DS-605, and cabozantinib. Additional examples of a ROS1 inhibitor are known in the art.

The phrase “dysregulation of a MET gene, a MET protein, or the expression or activity or level of any of the same” refers to a genetic mutation (e.g., a chromosomal translocation that results in the expression of a fusion protein including a MET kinase domain and a fusion partner, a mutation in a MET gene that results in the expression a MET protein that includes a deletion of at least one amino acid as compared to a wildtype MET protein, a mutation in a MET gene that results in the expression of a MET protein with one or more point mutations as compared to a wildtype MET protein, a mutation in a MET gene that results in the expression of a MET protein with at least one inserted amino acid as compared to a wildtype MET protein, a gene duplication that results in an increased level of MET protein in a cell, or a mutation in a regulatory sequence (e.g., a promoter and/or enhancer) that results in an increased level of MET protein in a cell), an alternative spliced version of a MET mRNA that results in a MET protein having a deletion of at least one amino acid in the MET protein as compared to the wild-type MET protein), or increased expression (e.g., increased levels) of a wildtype MET protein in a mammalian cell due to aberrant cell signaling and/or dysregulated autocrine/paracrine signaling (e.g., as compared to a control non-cancerous cell). As another example, a dysregulation of a MET gene, a MET protein, or expression or activity, or level of any of the same, can be a mutation in a MET gene that encodes a MET protein that is constitutively active or has increased activity as compared to a protein encoded by a MET gene that does not include the mutation. For example, a dysregulation of a MET gene, a MET protein, or expression or activity, or level of any of the same, can be the result of a gene or chromosome translocation which results in the expression of a fusion protein that contains a first portion of a MET protein that includes a functional kinase domain, and a second portion of a partner protein (i.e., that is not MET). In some examples, dysregulation of a MET gene, a MET protein, or expression or activity or level of any of the same can be a result of a gene translocation of one MET gene with another non-MET gene.

Non-limiting examples of a MET inhibitor include crizotinib, cabozantinib, JNJ-38877605, PF-04217903 (Pfizer), MK-2461, GSK 1363089, AMG 458 (Amgen), tivantinib, INCB28060 (Incyte), PF-02341066 (Pfizer), E7050 (Eisai), BMS-777607 (Bristol-Meyers Squibb), JNJ-38877605 (Johnson & Johnson), ARQ197 (ArQule), GSK/1363089/XL880 (GSK/Exeilixis), and XL174 (BMS/Exelixis). Additional examples of a MET inhibitor are known in the art.

The phrase “dysregulation of a aromatase gene, an aromatase protein, or the expression or activity or level of any of the same” refers to a genetic mutation (e.g., a mutation in an aromatase gene that results in the expression an aromatase protein that includes a deletion of at least one amino acid as compared to a wildtype aromatase protein, a mutation in an aromatase gene that results in the expression of an aromatase protein with one or more point mutations as compared to a wildtype aromatase protein, a mutation in an aromatase gene that results in the expression of an aromatase protein with at least one inserted amino acid as compared to a wildtype aromatase protein, a gene duplication that results in an increased level of aromatase protein in a cell, or a mutation in a regulatory sequence (e.g., a promoter and/or enhancer) that results in an increased level of aromatase protein in a cell), an alternative spliced version of an aromatase mRNA that results in an aromatase protein having a deletion of at least one amino acid in the aromatase protein as compared to the wild-type aromatase protein), or increased expression (e.g., increased levels) of a wildtype aromatase in a mammalian cell due to aberrant cell signaling and/or dysregulated autocrine/paracrine signaling (e.g., as compared to a control non-cancerous cell). As another example, a dysregulation of an aromatase gene, an aromatase protein, or expression or activity, or level of any of the same, can be a mutation in an aromatase gene that encodes an aromatase protein that is constitutively active or has increased activity as compared to a protein encoded by an aromatase gene that does not include the mutation.

Non-limiting examples of an aromatase inhibitor include Arimidex (anastrozole), Aromasin (exemestane), Femara (letrozole), Teslac (testolactone), and formestane. Additional examples of an aromatase inhibitor are known in the art.

The phrase “dysregulation of a RAF gene, a RAF protein, or the expression or activity or level of any of the same” refers to a genetic mutation (e.g., a chromosomal translocation that results in the expression of a fusion protein including a RAF kinase domain and a fusion partner, a mutation in a RAF gene that results in the expression a RAF protein that includes a deletion of at least one amino acid as compared to a wildtype RAF protein, a mutation in a RAF gene that results in the expression of a RAF protein with one or more point mutations as compared to a wildtype RAF protein, a mutation in a RAF gene that results in the expression of a RAF protein with at least one inserted amino acid as compared to a wildtype RAF protein, a gene duplication that results in an increased level of RAF protein in a cell, or a mutation in a regulatory sequence (e.g., a promoter and/or enhancer) that results in an increased level of RAF protein in a cell), an alternative spliced version of a RAF mRNA that results in a RAF protein having a deletion of at least one amino acid in the RAF protein as compared to the wild-type RAF protein), or increased expression (e.g., increased levels) of a wildtype RAF protein in a mammalian cell due to aberrant cell signaling and/or dysregulated autocrine/paracrine signaling (e.g., as compared to a control non-cancerous cell). As another example, a dysregulation of a RAF gene, a RAF protein, or expression or activity, or level of any of the same, can be a mutation in a RAF gene that encodes a RAF protein that is constitutively active or has increased activity as compared to a protein encoded by a RAF gene that does not include the mutation. For example, a dysregulation of a RAF gene, a RAF protein, or expression or activity, or level of any of the same, can be the result of a gene or chromosome translocation which results in the expression of a fusion protein that contains a first portion of a RAF protein that includes a functional kinase domain, and a second portion of a partner protein (i.e., that is not RAF). In some examples, dysregulation of a RAF gene, a RAF protein, or expression or activity or level of any of the same can be a result of a gene translocation of one RAF gene with another non-RAF gene.

Non-limiting examples of a RAF inhibitor include sorafenib, vemurafenib, dabrafenib, BMS-908662/XL281, GSK2118436, RAF265, R05126766, and R04987655. Additional examples of a RAF inhibitor are known in the art.

The phrase “dysregulation of a RAS gene, a RAS protein, or the expression or activity or level of any of the same” refers to a genetic mutation (e.g., a chromosomal translocation that results in the expression of a fusion protein including a RAS kinase domain and a fusion partner, a mutation in a RAS gene that results in the expression a RAS protein that includes a deletion of at least one amino acid as compared to a wildtype RAS protein, a mutation in a RAS gene that results in the expression of a RAS protein with one or more point mutations as compared to a wildtype RAS protein, a mutation in a RAS gene that results in the expression of a RAS protein with at least one inserted amino acid as compared to a wildtype RAS protein, a gene duplication that results in an increased level of RAS protein in a cell, or a mutation in a regulatory sequence (e.g., a promoter and/or enhancer) that results in an increased level of RAS protein in a cell), an alternative spliced version of a RAS mRNA that results in a RAS protein having a deletion of at least one amino acid in the RAS protein as compared to the wild-type RAS protein), or increased expression (e.g., increased levels) of a wildtype RAS protein in a mammalian cell due to aberrant cell signaling and/or dysregulated autocrine/paracrine signaling (e.g., as compared to a control non-cancerous cell). As another example, a dysregulation of a RAS gene, a RAS protein, or expression or activity, or level of any of the same, can be a mutation in a RAS gene that encodes a RAS protein that is constitutively active or has increased activity as compared to a protein encoded by a RAS gene that does not include the mutation. For example, a dysregulation of a RAS gene, a RAS protein, or expression or activity, or level of any of the same, can be the result of a gene or chromosome translocation which results in the expression of a fusion protein that contains a first portion of a RAS protein that includes a functional kinase domain, and a second portion of a partner protein (i.e., that is not RAS). In some examples, dysregulation of a RAS gene, a RAS protein, or expression or activity or level of any of the same can be a result of a gene translocation of one RAS gene with another non-RAS gene.

Non-limiting examples of a RAS inhibitor include Kobe0065 and Kobe2602. Additional examples of a RAS inhibitor are known in the art.

Non-limiting examples of multi-kinase inhibitors (MKIs) include dasatinib and sunitinib.

Also provided are methods of selecting a treatment for a subject having a cancer that include (a) administering one or more doses of a first RET inhibitor to the subject for a period of time; (b) after (a), determining whether a cancer cell in a sample obtained from the subject has at least one RET inhibitor resistance mutation; and (c) selecting a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof as a monotherapy or in conjunction with another anticancer agent for the subject if the subject has a cancer cell that has one or more RET inhibitor resistance mutations; or (d) selecting additional doses of the first RET inhibitor of step (a) for the subject if the subject has a cancer cell that does not have a RET inhibitor resistance mutation. In some embodiments, when additional doses of the first RET inhibitor of step (a) are selected for the subject, the method can further include selecting doses of another anticancer agent for the subject. In some embodiments, the one or more RET inhibitor resistance mutations confer increased resistance to a cancer cell or tumor to treatment with the first RET inhibitor. In some embodiments, the one or more RET inhibitor resistance mutations include one or more RET inhibitor resistance mutations listed in Tables 3 and 4. For example, the one or more RET inhibitor resistance mutations can include a substitution at amino acid position 804, e.g., V804M, V804L, or V804E. In some embodiments, the additional anticancer agent is any anticancer agent known in the art. For example, the additional anticancer agent is another RET inhibitor (e.g., a second RET inhibitor). In some embodiments, the additional anticancer agent is an immunotherapy. In some embodiments of step (c), another RET inhibitor can be the first RET inhibitor administered in step (a).

Also provided are methods of selecting a treatment for a subject having a cancer that include (a) administering one or more doses of a first RET inhibitor to the subject for a period of time; (b) after (a), determining whether a cancer cell in a sample obtained from the subject has at least one RET inhibitor resistance mutation; and (c) selecting a second RET inhibitor as a monotherapy or in conjunction with another anticancer agent if the subject has a cancer cell that has one or more RET inhibitor resistance mutations; or (d) selecting additional doses of the first RET inhibitor of step (a) for the subject if the subject has a cancer cell that does not have a RET inhibitor resistance mutation. In some embodiments, when additional doses of the first RET inhibitor of step (a) are selected for the subject, the method can further include selecting doses of another anticancer agent for the subject. In some embodiments, the one or more RET inhibitor resistance mutations confer increased resistance to a cancer cell or tumor to treatment with the first RET inhibitor. In some embodiments, the one or more RET inhibitor resistance mutations include one or more RET inhibitor resistance mutations listed in Tables 3 and 4. For example, the one or more RET inhibitor resistance mutations can include a substitution at amino acid position 804, e.g., V804M, V804L, or V804E. In some embodiments, the additional anticancer agent is any anticancer agent known in the art. For example, the additional anticancer agent is another RET inhibitor (e.g., a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof). In some embodiments, the additional anticancer agent is an immunotherapy. In some embodiments, another RET can be the first RET inhibitor administered in step (a).

Also provided are methods of selecting a treatment for a subject having a cancer that include (a) determining whether a cancer cell in a sample obtained from a subject having a cancer and previously administered one or more doses of a first RET inhibitor has one or more RET inhibitor resistance mutations; (b) selecting a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof as a monotherapy or in conjunction with another anticancer agent for the subject if the subject has a cancer cell that has at least one RET inhibitor resistance mutation; or (c) selecting additional doses of the first RET inhibitor previously administered to the subject if the subject has a cancer cell that does not have a RET inhibitor resistance mutation. In some embodiments, when additional doses of the first RET inhibitor previously administered to the subject are selected for the subject, the method can further include selecting doses of another anticancer agent (e.g., a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof. or an immunotherapy) for the subject. In some embodiments, the one or more RET inhibitor resistance mutations confer increased resistance to a cancer cell or tumor to treatment with the first RET inhibitor. In some embodiments, the one or more RET inhibitor resistance mutations include one or more RET inhibitor resistance mutations listed in Tables 3 and 4. For example, the one or more RET inhibitor resistance mutations can include a substitution at amino acid position 804, e.g., V804M, V804L, or V804E. In some embodiments, the additional anticancer agent is any anticancer agent known in the art. For example, the additional anticancer agent is another RET inhibitor (e.g., a second RET inhibitor). In some embodiments, the additional anticancer agent is an immunotherapy. In some embodiments of step (c), another RET inhibitor can be the first RET inhibitor administered in step (a).

Also provided are methods of selecting a treatment for a subject having a cancer that include (a) determining whether a cancer cell in a sample obtained from a subject having a cancer and previously administered one or more doses of a first RET inhibitor has one or more RET inhibitor resistance mutations; (b) selecting a second RET inhibitor as a monotherapy or in conjunction with another anticancer agent for the subject if the subject has a cancer cell that has at least one RET inhibitor resistance mutation; or (c) selecting additional doses of the first RET inhibitor previously administered to the subject if the subject has a cancer cell that does not have a RET inhibitor resistance mutation. In some embodiments, when additional doses of the first RET inhibitor previously administered to the subject are selected for the subject, the method can further include selecting doses of another anticancer agent (e.g., a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof, or an immunotherapy) for the subject. In some embodiments, the one or more RET inhibitor resistance mutations confer increased resistance to a cancer cell or tumor to treatment with the first RET inhibitor. In some embodiments, the one or more RET inhibitor resistance mutations include one or more RET inhibitor resistance mutations listed in Tables 3 and 4. For example, the one or more RET inhibitor resistance mutations can include a substitution at amino acid position 804, e.g., V804M, V804L, or V804E. In some embodiments, the additional anticancer agent is any anticancer agent known in the art. For example, the additional anticancer agent is another RET inhibitor (e.g., a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof). In some embodiments, the additional anticancer agent is an immunotherapy. In some embodiments, another RET can be the first RET inhibitor administered in step (a).

Also provided are methods of determining a subject's risk for developing a cancer that has some resistance to a first RET inhibitor that include: determining whether a cell in a sample obtained from the subject has one or more RET inhibitor resistance mutations; and identifying a subject having a cell that has one or more RET inhibitor resistance mutations, as having an increased likelihood of developing a cancer that has some resistance to the first RET inhibitor. Also provided are methods of determining a subject's risk for developing a cancer that has some resistance to a first RET inhibitor that include: identifying a subject having a cell that has one or more RET inhibitor resistance mutations, as having an increased likelihood of developing a cancer that has some resistance to the first RET inhibitor. Also provided are methods of determining the presence of a cancer that has some resistance to a first RET inhibitor that include: determining whether a cancer cell in a sample obtained from the subject has one or more RET inhibitor resistance mutations; and determining that the subject having a cancer cell that has one or more RET inhibitor resistance mutations has a cancer that has some resistance to the first RET inhibitor. Also provided are methods of determining the presence of a cancer that has some resistance to a first RET inhibitor in a subject that include: determining that a subject having a cancer cell that has one or more RET inhibitor resistance mutations, has a cancer that has some resistance to the first RET inhibitor. In some embodiments, the one or more RET inhibitor resistance mutations confer increased resistance to a cancer cell or tumor to treatment with the first RET inhibitor. In some embodiments, the one or more RET inhibitor resistance mutations include one or more RET inhibitor resistance mutations listed in Tables 3 and 4. For example, the one or more RET inhibitor resistance mutations can include a substitution at amino acid position 804, e.g., V804M, V804L, or V804E.

In some embodiments of any of the methods described herein, a RET inhibitor resistance mutation that confers increased resistance to a cancer cell or tumor to treatment with a first RET inhibitor can be any of the RET inhibitor resistance mutations listed in Table 3 or 4 (e.g., a substitution at amino acid position 804, e.g., V804M, V804L, or V804E).

In some embodiments, the presence of one or more RET inhibitor resistance mutations in a tumor causes the tumor to be more resistant to treatment with a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof. Methods useful when a RET inhibitor resistance mutation causes the tumor to be more resistant to treatment with a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof are described below. For example, provided herein are methods of treating a subject having a cancer that include: identifying a subject having a cancer cell that has one or more RET inhibitor resistance mutations; and administering to the identified subject a treatment that does not include a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof as a monotherapy (e.g., a second RET kinase inhibitor). Also provided are methods of treating a subject identified as having a cancer cell that has one or more RET inhibitor resistance mutations that include administering to the subject a treatment that does not include a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof as a monotherapy (e.g., a second RET kinase inhibitor). In some embodiments, the one or more RET inhibitor resistance mutations confer increased resistance to a cancer cell or tumor to treatment with a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof.

Also provided are methods of selecting a treatment for a subject having a cancer that include: identifying a subject having a cancer cell that has one or more RET inhibitor resistance mutations; and selecting a treatment that does not include a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof as a monotherapy for the identified subject (e.g., a second RET kinase inhibitor). Also provided are methods of selecting a treatment for a subject having a cancer that include: selecting a treatment that does not include a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof as a monotherapy (e.g., a second RET kinase inhibitor) for a subject identified as having a cancer cell that has one or more RET inhibitor resistance mutations. Also provided are methods of selecting a subject having a cancer for a treatment that does not include a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof as a monotherapy (e.g., a second RET kinase inhibitor) that include: identifying a subject having a cancer cell that has one or more RET inhibitor resistance mutations; and selecting the identified subject for a treatment that does not include a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof as a monotherapy (e.g., a second RET kinase inhibitor). Also provided are methods of selecting a subject having a cancer for a treatment that does not include a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof as a monotherapy (e.g., a second RET kinase inhibitor) that include: selecting a subject identified as having a cancer cell that has one or more RET inhibitor resistance mutations for a treatment that does not include a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof as a monotherapy. In some embodiments, the one or more RET inhibitor resistance mutations confer increased resistance to a cancer cell or tumor to treatment with a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof.

Also provided are methods of determining the likelihood that a subject having a cancer will have a positive response to treatment with a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof as a monotherapy that include: determining whether a cancer cell in a sample obtained from the subject has one or more RET inhibitor resistance mutations; and determining that the subject having the cancer cell that has one or more RET inhibitor resistance mutations has a decreased likelihood of having a positive response to treatment with a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof as a monotherapy. Also provided are methods of determining the likelihood that a subject having cancer will have a positive response to treatment with a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof as a monotherapy that include: determining that a subject having a cancer cell that has one or more RET inhibitor resistance mutations has a decreased likelihood of having a positive response to treatment with a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof as a monotherapy. Also provided are methods of predicting the efficacy of treatment with a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof as a monotherapy in a subject having cancer that include: determining whether a cancer cell in a sample obtained from the subject has one or more RET inhibitor resistance mutations; and determining that treatment with a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof as a monotherapy is less likely to be effective in a subject having a cancer cell in a sample obtained from the subject that has one or more RET inhibitor resistance mutations. Also provided are methods of predicting the efficacy of treatment with a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof as a monotherapy in a subject having cancer that include: determining that treatment with a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof as a monotherapy is less likely to be effective in a subject having a cancer cell in a sample obtained from the subject that has one or more RET inhibitor resistance mutations. In some embodiments, the one or more RET inhibitor resistance mutations confer increased resistance to a cancer cell or tumor to treatment with a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof.

Also provided are methods of treating a subject having a cancer that include: (a) administering one or more doses of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof for a period of time; (b) after (a), determining whether a cancer cell in a sample obtained from the subject has one or more RET inhibitor resistance mutations; and (c) administering a second RET inhibitor or a second compound of Formula I or a pharmaceutically acceptable salt or solvate thereof as a monotherapy or in conjunction with another anticancer agent to a subject having a cancer cell that has one or more RET inhibitor resistance mutations; or (d) administering additional doses of the compound of Formula I or a pharmaceutically acceptable salt or solvate thereof of step (a) to a subject having a cancer cell that does not have a RET inhibitor resistance mutation. In some embodiments, where the subject is administered additional doses of the compound of Formula I or a pharmaceutically acceptable salt or solvate thereof of step (a), the subject can also be administered another anticancer agent or a second compound of Formula I or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the one or more RET inhibitor resistance mutations confer increased resistance to a cancer cell or tumor to treatment with a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the additional anticancer agent is any anticancer agent known in the art. For example, the additional anticancer agent is another RET inhibitor (e.g., a second RET inhibitor). In some embodiments, the additional anticancer agent is an immunotherapy. In some embodiments, another RET can be the compound of Formula I or a pharmaceutically acceptable salt or solvate thereof administered in step (a).

Also provided are methods of treating a subject having a cancer that include: (a) determining whether a cancer cell in a sample obtained from a subject having a cancer and previously administered one or more doses of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof, has one or more RET inhibitor resistance mutations; (b) administering a second RET inhibitor or a second compound of Formula I or a pharmaceutically acceptable salt or solvate thereof as a monotherapy or in conjunction with another anticancer agent to a subject having a cancer cell that has one or more RET inhibitor resistance mutations; or (c) administering additional doses of the compound of Formula I or a pharmaceutically acceptable salt or solvate thereof previously administered to a subject having a cancer cell that does not have a RET inhibitor resistance mutation. In some embodiments, where the subject is administered additional doses of the compound of Formula I or a pharmaceutically acceptable salt or solvate thereof of step (a), the subject can also be administered another anticancer agent. In some embodiments, the one or more RET inhibitor resistance mutations confer increased resistance to a cancer cell or tumor to treatment with a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the additional anticancer agent is any anticancer agent known in the art. For example, the additional anticancer agent is another RET inhibitor (e.g., a second RET inhibitor). In some embodiments, the additional anticancer agent is an immunotherapy. In some embodiments, another RET can be the compound of Formula I or a pharmaceutically acceptable salt or solvate thereof administered in step (a).

Also provided are methods of selecting a treatment for a subject having a cancer that include: (a) administering one or more doses of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof to the subject for a period of time; (b) after (a), determining whether a cancer cell in a sample obtained from the subject has one or more RET inhibitor resistance mutations; and (c) selecting a second RET inhibitor or a second compound of Formula I or a pharmaceutically acceptable salt or solvate thereof as a monotherapy or in conjunction with another anticancer agent for the subject if the subject has a cancer cell that has a RET inhibitor resistance mutation; or (d) selecting additional doses of the compound of Formula I or a pharmaceutically acceptable salt or solvate thereof of step (a) for the subject if the subject has a cancer cell that does not have a RET inhibitor resistance mutation. In some embodiments, where additional doses of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof of step (a) are selected for the subject, the method can also include further selecting another anticancer agent. In some embodiments, the one or more RET inhibitor resistance mutations confer increased resistance to a cancer cell or tumor to treatment with a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the additional anticancer agent is any anticancer agent known in the art. For example, the additional anticancer agent is another RET inhibitor (e.g., a second RET inhibitor). In some embodiments, the additional anticancer agent is an immunotherapy. In some embodiments, another RET can be the compound of Formula I or a pharmaceutically acceptable salt or solvate thereof administered in step (a).

Also provided are methods of selecting a treatment for a subject having a cancer that include: (a) determining whether a cancer cell in a sample obtained from a subject having a cancer and previously administered one or more doses of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof, has one or more RET inhibitor resistance mutations; (b) selecting a second RET inhibitor or a second compound of Formula I or a pharmaceutically acceptable salt or solvate thereof as a monotherapy or in conjunction with another anticancer agent for the subject if the subject has a cancer cell that has a RET inhibitor resistance mutation; or (c) selecting additional doses of the compound of Formula I or a pharmaceutically acceptable salt or solvate thereof previously administered to the subject if the subject has a cancer cell that does not have a RET inhibitor resistance mutation. In some embodiments, where additional doses of the compound of Formula I or a pharmaceutically acceptable salt or solvate thereof of step (a) are selected for the subject, the method can also include further selecting another anticancer agent. In some embodiments, the one or more RET inhibitor resistance mutations confer increased resistance to a cancer cell or tumor to treatment with a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the additional anticancer agent is any anticancer agent known in the art. For example, the additional anticancer agent is another RET inhibitor (e.g., a second RET inhibitor). In some embodiments, the additional anticancer agent is an immunotherapy. In some embodiments, another RET can be the compound of Formula I or a pharmaceutically acceptable salt or solvate thereof administered in step (a).

Also provided are methods of determining a subject's risk for developing a cancer that has some resistance to a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof that include: determining whether a cell in a sample obtained from the subject has one or more RET inhibitor resistance mutations; and identifying the subject if the subject has a cell that has one or more RET inhibitor resistance mutations as having an increased likelihood of developing a cancer that has some resistance to a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof. Also provided are methods of determining a subject's risk for developing a cancer that has some resistance to a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof that include: identifying a subject having a cell that has one or more RET inhibitor resistance mutations as having an increased likelihood of developing a cancer that has some resistance to a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof. Also provided are methods of determining the presence of a cancer that has some resistance to a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof that includes: determining whether a cancer cell in a sample obtained from the subject has one or more RET inhibitor resistance mutations; and determining that the subject having the cancer cell that has one or more RET inhibitor resistance mutations has a cancer that has some resistance to a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof. Also provided are methods of determining the presence of a cancer that has some resistance to a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof in a subject that include: determining that a subject having a cancer cell that has one or more RET inhibitor resistance mutations has a cancer that has some resistance to a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, the one or more RET inhibitor resistance mutations confer increased resistance to a cancer cell or tumor to treatment with a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof.

In some embodiments of any of the methods described herein, a RET inhibitor resistance mutation that confers increased resistance to a cancer cell or tumor to treatment with a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof, can be any of the RET inhibitor resistance mutations listed in Table 3 or 4.

Methods of determining the level of resistance of a cancer cell or a tumor to a RET inhibitor (e.g., any of the RET inhibitors described herein or known in the art) can be determined using methods known in the art. For example, the level of resistance of a cancer cell to a RET inhibitor can be assessed by determining the IC₅₀ of a RET inhibitor (e.g., any of the RET inhibitors described herein or known in the art) on the viability of a cancer cell. In other examples, the level of resistance of a cancer cell to a RET inhibitor can be assessed by determining the growth rate of the cancer cell in the presence of a RET inhibitor (e.g., any of the RET inhibitors described herein). In other examples, the level of resistance of a tumor to a RET inhibitor can be assessed by determining the mass or size of one or more tumors in a subject over time during treatment with a RET inhibitor (e.g., any of the RET inhibitors described herein). In other examples, the level of resistance of a cancer cell or a tumor to a RET inhibitor can be indirectly assessed by determining the activity of a RET kinase including one or more of the RET inhibitor resistance mutations (i.e., the same RET kinase expressed in a cancer cell or a tumor in a subject). The level of resistance of a cancer cell or tumor having one or more RET inhibitor resistance mutations to a RET inhibitor is relative to the level of resistance in a cancer cell or tumor that does not have a RET inhibitor resistance mutation (e.g., a cancer cell or tumor that does not have the same RET inhibitor resistance mutations, a cancer cell or a tumor that does not have any RET inhibitor resistance mutations, or a cancer cell or a tumor that expresses a wildtype RET protein). For example, the determined level of resistance of a cancer cell or a tumor having one or more RET inhibitor resistance mutations can be greater than about 1%, greater than about 2%, greater than about 3%, greater than about 4%, greater than about 5%, greater than about 6%, greater than about 7%, greater than about 8%, greater than about 9%, greater than about 10%, greater than about 11%, greater than about 12%, greater than about 13%, greater than about 14%, greater than about 15%, greater than about 20%, greater than about 25%, greater than about 30%, greater than about 35%, greater than about 40%, greater than about 45%, greater than about 50%, greater than about 60%, greater than about 70%, greater than about 80%, greater than about 90%, greater than about 100%, greater than about 110%, greater than about 120%, greater than about 130%, greater than about 140%, greater than about 150%, greater than about 160%, greater than about 170%, greater than about 180%, greater than about 190%, greater than about 200%, greater than about 210%, greater than about 220%, greater than about 230%, greater than about 240%, greater than about 250%, greater than about 260%, greater than about 270%, greater than about 280%, greater than about 290%, or greater than about 300% of the level of resistance in a cancer cell or tumor that does not have a RET inhibitor resistance mutation (e.g., a cancer cell or tumor that does not have the same RET inhibitor resistance mutations, a cancer cell or a tumor that does not have any RET inhibitor resistance mutations, or a cancer cell or a tumor that expresses a wildtype RET protein).

RET is thought to play an important role in the development and survival of afferent nociceptors in the skin and gut. RET kinase knock-out mice lack enteric neurons and have other nervous system anomalies suggesting that a functional RET kinase protein product is necessary during development (Taraviras, S. et al., Development, 1999, 126:2785-2797). Moreover population studies of patients with Hirschsprung's disease characterized by colonic obstruction due to lack of normal colonic enervation have a higher proportion of both familial and sporadic loss of function RET mutations (Butler Tjaden N., et al., Transl. Res., 2013, 162: 1-15). Irritable bowel syndrome (IBS) is a common illness affecting 10-20% of individuals in developed countries and is characterized by abnormal bowel habits, bloating and visceral hypersensitivity (Camilleri, M., N. Engl. J. Med., 2012, 367: 1626-1635). While the etiology of IBS is unknown it is thought to result from either a disorder between the brain and gastrointestinal tract, a disturbance in the gut microbiome or increased inflammation. The resulting gastrointestinal changes affect normal bowel transit resulting in either diarrhea or constipation. Furthermore in many IBS patients the sensitization of the peripheral nervous system results in visceral hypersensitivity or allodynia (Keszthelyi, D., Eur. J. Pain, 2012, 16: 1444-1454). See, e.g., U.S. Publication No. 2015/0099762.

Accordingly, provided herein are methods for treating a patient diagnosed with (or identified as having) an irritable bowel syndrome (IBS) including diarrhea-predominant, constipation-predominant or alternating stool pattern, functional bloating, functional constipation, functional diarrhea, unspecified functional bowel disorder, functional abdominal pain syndrome, chronic idiopathic constipation, functional esophageal disorders, functional gastroduodenal disorders, functional anorectal pain, and inflammatory bowel disease that include administering to the patient a therapeutically effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof.

Also provided herein are methods for treating a patient identified or diagnosed as having a RET-associated irritable bowel syndrome (IBS) (e.g., a patient that has been identified or diagnosed as having a RET-associated irritable bowel syndrome (IBS) through the use of a regulatory agency-approved, e.g., FDA-approved, kit for identifying dysregulation of a RET gene, a RET kinase, or expression or activity or level of any of the same, in a patient or a biopsy sample from the patient) that include administering to the patient a therapeutically effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof.

Also provided herein are methods for treating pain associated with IBS that include administering to the patient a therapeutically effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof. In some embodiments, a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof is administered in combination with another therapeutic agent useful for treating one or more symptoms of IBS.

Also provided are methods for treating an irritable bowel syndrome (IBS) in a patient in need thereof, the method comprising: (a) determining if the irritable bowel syndrome (IBS) in the patient is a RET-associated IBS (e.g., using a regulatory-agency approved, e.g., FDA-approved, kit for identifying dysregulation of a RET gene, a RET kinase, or expression or activity or level of any of the same, in a patient or a biopsy sample from the patient, or by performing any of the non-limiting examples of assays described herein); and (b) if the IBS is determined to be a RET-associated IBS, administering to the patient a therapeutically effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof.

In some embodiments, the compounds of the present invention are useful for treating irritable bowel syndrome (IBS) in combination with one or more additional therapeutic agents or therapies effective in treating the irritable bowel syndrome that work by the same or a different mechanism of action. The at least one additional therapeutic agent may be administered with a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof as part of the same or separate dosage forms, via the same or different routes of administration, and on the same or different administration schedules according to standard pharmaceutical practice known to one skilled in the art.

Non-limiting examples of additional therapeutics for the treatment of irritable bowel syndrome (IBS) include probiotics, fiber supplements (e.g., psyllium, methylcellulose), anti-diarrheal medications (e.g., loperamide), bile acid binders (e.g., cholestyramine, colestipol, colesevelam), anticholinergic and antispasmodic medications (e.g., hyoscyamine, dicyclomine), antidepressant medications (e.g., tricyclic antidepressant such as imipramine or notriptyline or a selective serotonin reuptake inhibitor (SSRI) such as fluoxetine or paroxetine), antibiotics (e.g., rifaximin), alosetron, and lubiprostone.

Accordingly, also provided herein are methods of treating irritable bowel syndrome (IBS), comprising administering to a patient in need thereof a pharmaceutical combination for treating IBS which comprises (a) a compound of Formula I or pharmaceutically acceptable salt or solvate thereof, (b) an additional therapeutic agent, and (c) optionally at least one pharmaceutically acceptable carrier for simultaneous, separate or sequential use for the treatment of IBS, wherein the amounts of the compound of Formula I or pharmaceutically acceptable salt or solvate thereof and the additional therapeutic agent are together effective in treating the IBS. In one embodiment, the compound of Formula I or pharmaceutically acceptable salt or solvate thereof, and the additional therapeutic agent are administered simultaneously as separate dosages. In one embodiment, the compound of Formula I or pharmaceutically acceptable salt or solvate thereof, and the additional therapeutic agent are administered as separate dosages sequentially in any order, in jointly therapeutically effective amounts, e.g. in daily or intermittently dosages. In one embodiment, compound of Formula I or pharmaceutically acceptable salt or solvate thereof, and the additional therapeutic agent are administered simultaneously as a combined dosage.

Also provided herein is (i) a pharmaceutical combination for treating irritable bowel syndrome in a patient in need thereof, which comprises (a) a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof, (b) at least one additional therapeutic agent (e.g., any of the exemplary additional therapeutic agents described herein for treating irritable bowel syndrome or known in the art), and (c) optionally at least one pharmaceutically acceptable carrier for simultaneous, separate or sequential use for the treatment of irritable bowel syndrome, wherein the amounts of the compound of Formula I or pharmaceutically acceptable salt or solvate thereof and of the additional therapeutic agent are together effective in treating the irritable bowel syndrome; (ii) a pharmaceutical composition comprising such a combination; (iii) the use of such a combination for the preparation of a medicament for the treatment of irritable bowel syndrome; and (iv) a commercial package or product comprising such a combination as a combined preparation for simultaneous, separate or sequential use; and to a method of treatment of irritable bowel syndrome in a patient in need thereof. In one embodiment the patient is a human.

The term “pharmaceutical combination”, as used herein, refers to a pharmaceutical therapy resulting from the mixing or combining of more than one active ingredient and includes both fixed and non-fixed combinations of the active ingredients. The term “fixed combination” means that a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof and at least one additional therapeutic agent (e.g., an agent effective in treating irritable bowel syndrome), are both administered to a patient simultaneously in the form of a single composition or dosage. The term “non-fixed combination” means that a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof and at least one additional therapeutic agent (e.g., an agent effective in treating irritable bowel syndrome) are formulated as separate compositions or dosages, such that they may be administered to a patient in need thereof simultaneously, concurrently or sequentially with variable intervening time limits, wherein such administration provides effective levels of the two or more compounds in the body of the patient. In one embodiment, the compound of Formula I and the additional therapeutic agent are formulated as separate unit dosage forms, wherein the separate dosages forms are suitable for either sequential or simultaneous administration. These also apply to cocktail therapies, e.g. the administration of three or more active ingredients.

In some embodiments, a compound provided herein can be used as an agent for supportive care for a patient undergoing cancer treatment. For example, a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof, can be useful to reduce one or more symptoms associated with treatment with one or more cancer therapies such as diarrheal or constipations complications and/or abdominal pain. See, for example, U.S. Publication No. 2015/0099762 and Hoffman, J. M. et al. Gastroenterology (2012) 142:844-854. Accordingly, a compound, or a pharmaceutically acceptable salt thereof, or composition provided herein can be administered to a patient to address one or more complications associated with cancer treatment (e.g., gastrointestinal complications such as diarrhea, constipation, or abdominal pain).

In some embodiments, a therapeutically effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof, can be administered to a patient undergoing cancer treatment (e.g., a patient experiencing an adverse event associated with cancer treatment such as an immune-related adverse event or a gastrointestinal complication including diarrhea, constipation, and abdominal pain). For example, a compound provided herein, or a pharmaceutically acceptable salt thereof, can be used in the treatment of colitis or IBS associated with administration of a checkpoint inhibitor; see, e.g., Postow, M. A. et al. Journal of Clinical Oncology (2015) 33: 1974-1982. In some such embodiments, a compound provided herein, or a pharmaceutically acceptable salt thereof, can be formulated to exhibit low bioavailability and/or be targeted for delivery in the gastrointestinal tract. See, for example, U.S. Pat. No. 6,531,152.

Also provided is a method for inhibiting RET kinase activity in a cell, comprising contacting the cell with a compound of Formula I. In one embodiment, the contacting is in vitro. In one embodiment, the contacting is in vivo. In one embodiment, the contacting is in vivo, wherein the method comprises administering an effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof to a subject having a cell having RET kinase activity. In some embodiments, the cell is a cancer cell. In one embodiment, the cancer cell is any cancer as described herein. In some embodiments, the cancer cell is a RET-associated cancer cell. In some embodiments, the cell is a gastrointestinal cell.

Also provided is a method for inhibiting RET kinase activity in a mammalian cell, comprising contacting the cell with a compound of Formula I. In one embodiment, the contacting is in vitro. In one embodiment, the contacting is in vivo. In one embodiment, the contacting is in vivo, wherein the method comprises administering an effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof to a mammal having a cell having RET kinase activity. In some embodiments, the mammalian cell is a mammalian cancer cell. In one embodiment, the mammalian cancer cell is any cancer as described herein. In some embodiments, the mammalian cancer cell is a RET-associated cancer cell. In some embodiments, the mammalian cell is a gastrointestinal cell.

As used herein, the term “contacting” refers to the bringing together of indicated moieties in an in vitro system or an in vivo system. For example, “contacting” a RET kinase with a compound provided herein includes the administration of a compound provided herein to an individual or patient, such as a human, having a RET kinase, as well as, for example, introducing a compound provided herein into a sample containing a cellular or purified preparation containing the RET kinase.

Also provided herein is a method of inhibiting cell proliferation, in vitro or in vivo, the method comprising contacting a cell with an effective amount of a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof, or a pharmaceutical composition thereof as defined herein.

The phrase “effective amount” means an amount of compound that, when administered to a patient in need of such treatment, is sufficient to (i) treat a RET kinase-associated disease or disorder, (ii) attenuate, ameliorate, or eliminate one or more symptoms of the particular disease, condition, or disorder, or (iii) delay the onset of one or more symptoms of the particular disease, condition, or disorder described herein. The amount of a compound of Formula I that will correspond to such an amount will vary depending upon factors such as the particular compound, disease condition and its severity, the identity (e.g., weight) of the patient in need of treatment, but can nevertheless be routinely determined by one skilled in the art.

When employed as pharmaceuticals, the compounds of Formula I can be administered in the form of pharmaceutical compositions. These compositions can be prepared in a manner well known in the pharmaceutical art, and can be administered by a variety of routes, depending upon whether local or systemic treatment is desired and upon the area to be treated. Administration may be topical (including transdermal, epidermal, ophthalmic and to mucous membranes including intranasal, vaginal and rectal delivery), pulmonary (e.g., by inhalation or insufflation of powders or aerosols, including by nebulizer; intratracheal or intranasal), oral or parenteral. Oral administration can include a dosage form formulated for once-daily or twice-daily (BID) administration. Parenteral administration includes intravenous, intraarterial, subcutaneous, intraperitoneal intramuscular or injection or infusion; or intracranial, e.g., intrathecal or intraventricular, administration. Parenteral administration can be in the form of a single bolus dose, or may be, for example, by a continuous perfusion pump. Pharmaceutical compositions and formulations for topical administration may include transdermal patches, ointments, lotions, creams, gels, drops, suppositories, sprays, liquids and powders. Conventional pharmaceutical carriers, aqueous, powder or oily bases, thickeners and the like may be necessary or desirable.

Also provided herein are pharmaceutical compositions which contain, as the active ingredient, a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof, in combination with one or more pharmaceutically acceptable carriers (excipients). In some embodiments, the composition is suitable for topical administration. In making the compositions provided herein, the active ingredient is typically mixed with an excipient, diluted by an excipient or enclosed within such a carrier in the form of, for example, a capsule, sachet, paper, or other container. When the excipient serves as a diluent, it can be a solid, semi-solid, or liquid material, which acts as a vehicle, carrier or medium for the active ingredient. Thus, the compositions can be in the form of tablets, pills, powders, lozenges, sachets, cachets, elixirs, suspensions, emulsions, solutions, syrups, aerosols (as a solid or in a liquid medium), ointments containing, for example, up to 10% by weight of the active compound, soft and hard gelatin capsules, suppositories, sterile injectable solutions, and sterile packaged powders. In one embodiment, the composition is formulated for oral administration. In one embodiment, the composition is formulated as a tablet or capsule.

The compositions comprising a compound of Formula I or a pharmaceutically acceptable salt or solvate thereof can be formulated in a unit dosage form, each dosage containing from about 5 to about 1,000 mg (1 g), more usually about 100 mg to about 500 mg, of the active ingredient. The term “unit dosage form” refers to physically discrete units suitable as unitary dosages for human subjects and other patients, each unit containing a predetermined quantity of active material (i.e., a compound for Formula I as provided herein) calculated to produce the desired therapeutic effect, in association with a suitable pharmaceutical excipient.

In some embodiments, the compositions provided herein contain from about 5 mg to about 50 mg of the active ingredient. One having ordinary skill in the art will appreciate that this embodies compounds or compositions containing about 5 mg to about 10 mg, about 10 mg to about 15 mg, about 15 mg to about 20 mg, about 20 mg to about 25 mg, about 25 mg to about 30 mg, about 30 mg to about 35 mg, about 35 mg to about 40 mg, about 40 mg to about 45 mg, or about 45 mg to about 50 mg of the active ingredient.

In some embodiments, the compositions provided herein contain from about 50 mg to about 500 mg of the active ingredient. One having ordinary skill in the art will appreciate that this embodies compounds or compositions containing about 50 mg to about 100 mg, about 100 mg to about 150 mg, about 150 mg to about 200 mg, about 200 mg to about 250 mg, about 250 mg to about 300 mg, about 350 mg to about 400 mg, or about 450 mg to about 500 mg of the active ingredient.

In some embodiments, the compositions provided herein contain from about 500 mg to about 1,000 mg of the active ingredient. One having ordinary skill in the art will appreciate that this embodies compounds or compositions containing about 500 mg to about 550 mg, about 550 mg to about 600 mg, about 600 mg to about 650 mg, about 650 mg to about 700 mg, about 700 mg to about 750 mg, about 750 mg to about 800 mg, about 800 mg to about 850 mg, about 850 mg to about 900 mg, about 900 mg to about 950 mg, or about 950 mg to about 1,000 mg of the active ingredient.

The active compound may be effective over a wide dosage range and is generally administered in a pharmaceutically effective amount. It will be understood, however, that the amount of the compound actually administered will usually be determined by a physician, according to the relevant circumstances, including the condition to be treated, the chosen route of administration, the actual compound administered, the age, weight, and response of the individual patient, the severity of the patient's symptoms, and the like.

In some embodiments, the compounds provided herein can be administered in an amount ranging from about 1 mg/kg to about 100 mg/kg. In some embodiments, the compound provided herein can be administered in an amount of about 1 mg/kg to about 20 mg/kg, about 5 mg/kg to about 50 mg/kg, about 10 mg/kg to about 40 mg/kg, about 15 mg/kg to about 45 mg/kg, about 20 mg/kg to about 60 mg/kg, or about 40 mg/kg to about 70 mg/kg. For example, about 5 mg/kg, about 10 mg/kg, about 15 mg/kg, about 20 mg/kg, about 25 mg/kg, about 30 mg/kg, about 35 mg/kg, about 40 mg/kg, about 45 mg/kg, about 50 mg/kg, about 55 mg/kg, about 60 mg/kg, about 65 mg/kg, about 70 mg/kg, about 75 mg/kg, about 80 mg/kg, about 85 mg/kg, about 90 mg/kg, about 95 mg/kg, or about 100 mg/kg. In some embodiments, such administration can be once-daily or twice-daily (BID) administration.

Provided herein are pharmaceutical kits useful, for example, in the treatment of RET-associated diseases or disorders, such as cancer or irritable bowel syndrome (IBS), which include one or more containers containing a pharmaceutical composition comprising a therapeutically effective amount of a compound provided herein. Such kits can further include, if desired, one or more of various conventional pharmaceutical kit components, such as, for example, containers with one or more pharmaceutically acceptable carriers, additional containers, etc., as will be readily apparent to those skilled in the art. Instructions, either as inserts or as labels, indicating quantities of the components to be administered, guidelines for administration, and/or guidelines for mixing the components, can also be included in the kit.

One skilled in the art will recognize that, both in vivo and in vitro trials using suitable, known and generally accepted cell and/or animal models are predictive of the ability of a test compound to treat or prevent a given disorder.

One skilled in the art will further recognize that human clinical trials including first-in-human, dose ranging and efficacy trials, in healthy patients and/or those suffering from a given disorder, may be completed according to methods well known in the clinical and medical arts.

EXAMPLES

The following examples illustrate the invention.

Biological Examples Example A RET Enzyme Assay

Compounds of Formula I were screened for their ability to inhibit wildtype and V804M mutant RET kinase using CisBio's HTRF® KinEASE™-TK assay technology. Briefly, N-terminal GST tagged recombinant human RET cytoplasmic domain (aa 658-end) from Eurofins (0.25 nM RET; Catalog No. 14-570M) or N-terminal GST tagged recombinant human V804M mutant RET cytoplasmic domain (aa 658-end) from Millipore (0.25 nM enzyme; Catalog No. 14-760) was incubated with 250 nM TK-substrate biotin (CisBio, part of Catalog No. 62TK0PEC) and 1 mM ATP along with test compound in a buffer consisting of 25 mM HEPES pH 7.4, 10 mM MgCl₂, 0.01% Triton X-100, and 2% DMSO in a volume of 8 μL. Compounds were typically prepared in a threefold serial dilution in DMSO and added to the assay to give the appropriate final concentration. After a 30-minute incubation at 22° C., the reaction was quenched by adding 8 μL of quench solution containing 31.25 nM Sa-XL665 and 1×TK-ab-Cryptate in HTRF detection buffer (all from CisBio, part of Cat. No. 62TK0PEC). After a 1 hour incubation at 22° C., the extent of reaction was determined using a PerkinElmer EnVision multimode plate reader via HTRF dual wavelength detection, and the percent of control (POC) was calculated using a ratiometric emission factor. 100 POC was determined using no test compounds and 0 POC was determined using pre-quenched control reactions. The POC values were fit to a 4 parameter logistic curve, and the IC₅₀ is defined as the concentration of inhibitor at which the POC equals 50 for the fitted curve. The IC₅₀ values for the compounds tested in this assay are provided in Table 5.

Example B

RET Cell Assay

The cellular potency of a compound inhibiting RET kinase was determined in HEK-293 cells expressing a Kif5b-RET fusion protein. Briefly, HEK-293 cells expressing a Kif5b-RET fusion protein were plated at 50K cells/well in 96 well poly-D-Lysine coated plates the day prior to the assay. The cells were incubated for 1 hour with test compound in DMEM (Dulbecco's Modified Eagle Medium) at a final DMSO concentration of 0.5%. Compounds were typically prepared in a three-fold serial dilution in DMSO and added to the assay to give the appropriate final concentration. After 1 hour the media was removed, the cells were fixed with 3.8% formaldehyde for 20 min, washed with PBS, and permeabilized for 10 min with 100% methanol. The plates were then washed with PBS-0.05% Tween20, and blocked with LI-COR Blocking solution (LI-COR catalog #927-40000) for 1 hour. Plates were washed with PBS-0.05% Tween20, then incubated with anti-phospho-RET(Tyr1062) (Santa Cruz catalog #sc-20252-R) antibody and anti-GAPDH (Millipore catalog #MAB374) antibody for 2 hours. The plates were washed with PBS-0.05% Tween20, and incubated with anti-rabbit 680 (Molecular Probes catalog No. A21109) and anti-mouse 800 (LI-COR catalog No. 926-32210) secondary antibodies for 1 hour. All antibodies were diluted in LI-COR Block containing 0.05% Tween. The plates were washed with PBS-0.05% Tween20, 100 μL PBS was added to each well, and the plates were read on a LI-COR Aerius fluorescent plate reader. The phospho-RET signal was normalized to the GAPDH signal. 100 POC (percent of control) was determined using no test compounds and 0 POC was determined using 1 μM of a control inhibitor. The POC values were fit to a 4 parameter logistic curve. The IC₅₀ value is the point where the curve crosses 50 POC. The IC₅₀ values for the compounds tested in this assay are provided in Table 5.

TABLE 5 IC₅₀'s of compounds tested in the assay of Examples A and B RET Enzyme RET enzyme KIF5B-RET (wild type) (V804M) pTYR1062 Cell Ex# IC₅₀ (nM) IC₅₀ (nM) IC₅₀ (nM) 1 368.8 N/A N/A 2 36.4 N/A 62.7 3 52.2 N/A 153.1 4 64.5 39.4 209.9 5 23.7 56.4 35.4 6 42.7 100.6 72.6 7 141.3 1095.6 N/A 8 144.2 1006.7 N/A 9 10.1 N/A 27.8 10 35.0 N/A 70.7 11 18.6 79.9 20.7 12 5.2 17.1 7.0 13 14.1 N/A 30.0 14 11.2 37.6 8.9 15 24.9 88.3 24.3 16 70.0 309.5 84.2 17 30.4 91.7 25.8 18 10.7 56.7 7.3 19 12.3 117.0 28.5 20 30.2 159.7 27.6 21 54.6 308.8 74.2 22 73.1 343.8 84.1 23 5.5 16.6 5.3 24 20.9 67.6 11.0 25 16.4 83.8 12.9 26 168.0 924.0 N/A 27 7.1 14.0 7.0 28 13.2 18.5 6.5 29 16.6 41.3 10.7 30 16.8 164.0 32.0 31 162.0 927.5 N/A 32 21.6 75.6 7.0 33 77.2 352.1 52.2 34 138.6 624.2 N/A 35 25.7 112.8 16.7 36 39.3 179.3 31.0 37 52.4 435.5 88.2 38 9.0 29.6 7.7 39 17.0 91.0 14.4 40 4.5 31.8 2.7 41 142.1 875.2 N/A 42 8.3 16.6 5.2 43 39.3 208.7 102.1 44 4195.9 10000.0 N/A 45 53.0 414.6 57.5 46 31.1 335.2 15.4 47 13.8 58.4 17.6 48 19.0 47.5 21.5 49 25.5 83.3 9.1 50 7.0 22.4 5.0 51 26.6 68.6 6.4 52 8.9 29.6 3.8 53 6.8 28.1 4.0 54 18.9 64.3 6.2 55 31.5 112.8 16.6 56 26.0 61.9 7.1 57 40.8 105.1 21.9 58 32.4 47.2 75.4 59 16.8 29.0 24.4 60 9.9 76.1 21.1 62 13.1 60.7 24.0 63 2.8 18.0 12.2 64 4.2 20.8 6.9 65 13.9 66.2 21.4 67 13.1 190.7 67.9 68 6.6 26.3 69.6 69 19.4 369.8 146.0 70 292.2 1914.2 N/A 71 154.2 1324.1 N/A 72 24.8 179.5 778.5 73 127.1 504.4 N/A 74 31.3 83.7 188.6 75 11.4 192.3 53.2 76 59.7 500.0 350.7 77 9.3 46.6 6.2 78 10.5 28.1 4.2 79 5.7 45.1 22.7 80 23.0 86.5 29.7 81 223.6 2344.3 N/A 82 29.6 215.8 37.2 83 34.9 280.0 106.9 84 386.4 2757.1 N/A 85 284.6 2617.1 N/A 86 43.9 342.7 181.5 87 123.4 998.6 N/A 88 20.0 104.4 14.1 89 11.1 55.5 20.7 90 42.5 193.2 79.8 91 49.7 479.2 20.3 92 17.8 78.1 12.4 93 28.4 61.3 5.6 94 6.5 13.7 2.7 95 25.9 152.0 33.9 96 27.5 229.9 25.8 97 150.8 1382.2 N/A 98 4.4 5.8 2.1 99 4.8 9.0 2.9 100 7.1 11.7 2.3 101 3.9 8.7 2.3 102 7.2 20.1 4.8 103 112.9 2526.4 N/A 104 84.3 711.7 164.1 105 735.4 10000.0 N/A 106 112.0 957.6 N/A 107 130.2 420.0 N/A 108 247.9 849.5 N/A 109 11.0 51.4 7.8 110 85.7 1581.2 302.1 111 33.3 209.7 131.7 112 30.7 229.3 61.7 113 224.9 1328.0 N/A 114 68.5 1267.9 198.5 115 55.1 856.0 79.3 116 223.0 3846.9 1068.7 117 121.2 699.5 N/A 118 19.8 34.8 6.4 119 47.7 364.3 83.1 120 57.4 320.9 82.6 121 31.7 273.4 63.8

Synthetic Examples

Synthesis of Synthetic Intermediates

4-Chloro-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine hydrochloride

Step 1: Preparation of Diethyl 1-(2-(1-methyl-1H-pyrazol-4-yl)-2-oxoethyl)-1H-pyrazole-3,5-dicarboxylate. In 250 mL of acetonitrile was dissolved 2-chloro-1-(1-methyl-1H-pyrazol-4-yl)ethanone (18.3 g, 115 mmol) and diethyl 1H-pyrazole-3,5-dicarboxylate (24.5 g, 115 mmol) before finely ground K₂CO₃ (31.9 g, 231 mmol) was added in one portion. The reaction mixture was stirred at ambient temperature overnight. The reaction mixture was filtered, and the cake was washed with acetonitrile (100 mL). The filtrate was concentrated in vacuo to a thick oil. The oil was dissolved in EtOAc (80 mL), and heptane (200 mL) was added slowly with stirring. The resultant solids were stirred for 2 h, then filtered and washed with heptane. The solids were dried in a vacuum oven to afford the title compound (26.4 g, 67% yield).

Step 2: Preparation of Ethyl 4-hydroxy-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-2-carboxylate and 4-Hydroxy-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-2-carboxylic acid. In 320 mL of acetic acid were combined diethyl 1-(2-(1-methyl-1H-pyrazol-4-yl)-2-oxoethyl)-1H-pyrazole-3,5-dicarboxylate (8.0 g, 23.9 mmol) and NH₄OAc (55.3 g, 718 mmol) in a 500 mL glass pressure vessel. The vessel was sealed and the reaction mixture was heated to 120° C. overnight, followed by heating at 160° C. for 48 hours. The reaction mixture was cooled to ambient temperature and then poured into a 2 L flask. Water (960 mL) was slowly added and the mixture was stirred with cooling for 2 hours. The fine pink suspension that resulted after stirring overnight was collected by vacuum filtration. The solids were collected and dried in a vacuum oven to afford a 1:2 mixture of the title compounds, ethyl 4-hydroxy-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-2-carboxylate (5.45 g, 26% yield) and 4-hydroxy-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-2-carboxylic acid (5.45 g, 58% yield).

Step 3: Preparation of 6-(1-Methyl-1H-pyrazol-4-yl)-4-oxo-4,5-dihydropyrazolo[1,5-a]pyrazine-2-carboxylic acid. Crude ethyl 4-hydroxy-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-2-carboxylate (10.00 g, 34.81 mmol) was charged to a 500 mL flask equipped with mechanical stirring, a thermocouple, and a reflux condenser equipped with a nitrogen balloon. 6 N HCl (100 mL) was added, and the reaction mixture was heated at 65° C. for 32 h. The reaction mixture was cooled to ambient temperature overnight, and water (100 mL) was added. The reaction mixture was stirred for 1 h, and then filtered. The resulting solids were rinsed with water and dried in the vacuum oven overnight to afford the title compound (8.8 g, 98% yield).

Step 4: Preparation of 6-(1-Methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4 (5H)-one. 6-(1-Methyl-1H-pyrazol-4-yl)-4-oxo-4,5-dihydropyrazolo[1,5-a]pyrazine-2-carboxylic acid (10.0 g, 38.6 mmol) was added to a 500 mL flask equipped with mechanical stirring, a thermocouple, a reflux condenser and static nitrogen pressure. Cu(OAc)₂ (3.5 g, 19.3 mmol), 1,10-phenanthroline (3.5 g, 19.3 mmol) and N-methylpyrrolidone (100 mL) were added. The reaction mixture was heated to 165° C. overnight. The reaction mixture was cooled to ambient temperature, and 3 M HCl (200 mL) was added to afford a slurry, which was stirred overnight. The product was collected by vacuum filtration, rinsed with water, and dried in the vacuum oven overnight to afford the title compound (8.0 g, 96% yield).

Step 5: Preparation of 4-Chloro-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine hydrochloride. To a 100 mL 3-neck flask fitted with a magnetic stir bar, internal temperature probe, and reflux condenser was added 6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4 (5H)-one (5.0 g, 23.2 mmol), followed by phosphoryl trichloride (34.6 mL, 371 mmol). The reaction mixture was heated to 80° C. under nitrogen for 7 h. The reaction mixture was cooled to 50° C., then charged with 40 mL of acetonitrile, and cooled to ambient temperature. The resulting solids were filtered, washed with 20 mL of acetonitrile, and dried in a vacuum oven to afford the title compound (2.65 g). The filtrates were diluted with 80 mL of methyl tert-butyl ether and the reaction mixture was stirred at ambient temperature overnight. The resultant solids were filtered and dried to afford additional amounts of the title compound (2.97 g). The total yield of 4-chloro-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine hydrochloride was 4.55 g (16.8 mmol, 72.5% yield).

4-Chloro-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

Step 1: Preparation of 4-Chloro-3-iodo-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine. Under a N_(2(g)) atmosphere, a mixture of 4-chloro-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine (80.2 g, 343 mmol) and NIS (92.7 g, 412 mmol) in DMF (2000 mL) was mechanically stirred for 30 min at ambient temperature. Additional NIS (92.7 g, 412 mmol) was introduced as a solution in DMF (350 mL). The mixture was stirred for an additional 30 min at ambient temperature, then for 90 min at 50° C., before cooling to ambient temperature over 16 h. The resulting slurry was filtered, and the filter cake was rinsed with EtOAc (400 mL) and dried in a vacuum oven overnight at 40° C. to afford the title compound (87 g, 71% yield). MS (apci) m/z=359.96 (M+1), 361.96 (M+2).

Step 2: Preparation of 4-Chloro-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile. Under a N_(2(g)) atmosphere, a cold (−20 to −25° C.) slurry of 4-chloro-3-iodo-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine (43.0 g, 120 mmol) in THF (430 mL) was treated slowly with 1.65 M i-PrMgCl in THF (76.1 mL, 125.6 mmol) while maintaining the internal temperature at or below −19° C. during the addition. After stirring 20 min at −25° C., additional i-PrMgCl (2 mL, 3.3 mmol; 1.65 M) was introduced, and the reaction was stirred for 2 min at −25° C. Immediately thereafter, a solution of 1-cyanato-4-methoxybenzene (21.65 g, 138.3 mmol) in THF (60 mL) was introduced at a rate that allowed internal temperature to be maintained at or below −19° C. during the addition. The reaction was allowed to warm to 20° C. over 16 h, and the resultant slurry was filtered. The filter cake was rinsed with EtOAc (70 mL), then dried in a vacuum oven for 2 h at 40° C. to afford the title compound (22.2 g, 72% yield). MS (apci) m/z=258.8 (M+H). 1H NMR (400 MHz, DMSO-d₆) δ: 9.41 (s, 1H), 8.82 (s, 1H), 8.32 (s, 1H), 8.06 (s, 1H), 3.87 (s, 3H).

4-Chloro-6-(1-(4-methoxybenzyl)-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine hydrochloride

Step 1: Preparation of 4-Iodo-1-(4-methoxybenzyl)-1H-pyrazole. 4-Iodo-1H-pyrazole (5.0 g, 25.8 mmol) was dissolved in DMF (50 mL), and K₂CO₃ (4.27 g, 30.9 mmol) was added followed by 1-(chloromethyl)-4-methoxybenzene (3.86 mL, 28.4 mmol). The reaction mixture was stirred at ambient temperature overnight. The reaction mixture was then poured into water and extracted with Et₂O, washed with brine, dried over sodium sulfate, filtered, and concentrated to afford the title compound (8.3 g, 103% yield)

Step 2: Preparation of 2-Chloro-1-(1-(4-methoxybenzyl)-1H-pyrazol-4-yl)ethanone. 4-Iodo-1-(4-methoxybenzyl)-1H-pyrazole (8.1 g, 26 mmol) was dissolved in THF (50 mL) and cooled in an ice bath. Isopropylmagnesium chloride (2.9 M, 8.9 mL, 26 mmol) was added slowly. The reaction mixture was stirred for 10 min, and then 2-chloro-N-methoxy-N-methylacetamide (3.5 g, 26 mmol) dissolved in THF (15 mL) was added slowly by syringe. The reaction mixture was warmed to ambient temperature and stirred for 1 h. The reaction mixture was partitioned between EtOAc and 1N HCl, and the organic layer was dried over sodium sulfate, filtered, and concentrated to afford the crude title compound (7.1 g, 104% yield) as an amber oil that slowly solidified.

Step 3: Preparation of Diethyl 1-(2-(1-(4-methoxybenzyl)-1H-pyrazol-4-yl)-2-oxoethyl)-1H-pyrazole-3,5-dicarboxylate. Crude 2-chloro-1-(1-(4-methoxybenzyl)-1H-pyrazol-4-yl)ethanone (7.1 g, 21 mmol) was dissolved in acetonitrile (100 mL). Diethyl 1H-pyrazole-3,5-dicarboxylate (4.6 g, 21 mmol) was added, followed by K₂CO₃ (5.9 g, 43 mmol), and the reaction mixture was stirred at 45° C. for 1 h. The reaction mixture was cooled to ambient temperature, diluted with EtOAc, filtered, and concentrated. The residue was purified over silica gel to afford the title compound (8.7 g, 92% yield) as a white solid

Step 4: Preparation of Ethyl 4-hydroxy-6-(1-(4-methoxybenzyl)-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-2-carboxylate. Diethyl 1-(2-(1-(4-methoxybenzyl)-1H-pyrazol-4-yl)-2-oxoethyl)-1H-pyrazole-3,5-dicarboxylate (8.2 g, 18.6 mmol) was dissolved in HOAc (100 mL) and NH₄OAc (43.1 g, 559 mmol) was added. The reaction mixture heated in a sealed tube at 120° C. for 48 h. The reaction mixture was cooled to ambient temperature, poured into water (200 mL), filtered and dried to afford the title compound (5.65 g, 77% yield) as a white solid

Step 5: Preparation of 4-Hydroxy-6-(1-(4-methoxybenzyl)-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-2-carboxylic acid. Ethyl 4-hydroxy-6-(1-(4-methoxybenzyl)-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-2-carboxylate (5.4 g, 14 mmol) was suspended in THF (60 mL), and 1M lithium hydroxide (30 mL, 30 mmol) was added. The reaction mixture was heated to 50° C. for 30 min. The reaction mixture was quenched with slow addition of 1M HCl (35 mL) with vigorous stirring. Additional water (10 mL) was added to aid in stirring. The mixture was stirred vigorously at 50° C. for 15 min, then cooled and filtered. The isolated solids were washed with water and dried in vacuum oven to afford the title compound (4.6 g, 92% yield) as a white solid

Step 6: Preparation of 6-(1-(4-Methoxybenzyl)-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-ol. 4-Hydroxy-6-(1-(4-methoxybenzyl)-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-2-carboxylic acid (4.6 g, 13 mmol) was charged to a 25 mL flask and 1,10-phenanthroline (1.00 g, 5.5 mmol) and diacetoxycopper (1.0 g, 5.5 mmol) were added. The reaction mixture was diluted with N-methylpyrrolidone (12 mL) and then heated to 165° C. under nitrogen for 6 h. The reaction mixture was cooled to ambient temperature overnight, transferred to a flask with 1N HCl (20 mL) and stirred at 50° C. for 45 min. The reaction mixture was then filtered, and the isolated solids were washed with water and dried in vacuum oven to afford 4.7 g of a dark brown solid. The dried solid was suspended in 1N HCl (60 mL), and N-methylpyrrolidone (10 mL) was added to aid in wetting. The mixture was stirred at 65° C. for 1 h. The mixture was filtered and the isolated solids were washed with water until the resulting filtrate was colorless. The isolated solids were dried in vacuum oven to afford the title compound (3.7 g, 91% yield) as a brown solid.

Step 7: Preparation of 4-Chloro-6-(1-(4-methoxybenzyl)-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine hydrochloride. 6-(1-(4-Methoxybenzyl)-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-ol (3.7 g, 11.5 mmol) was suspended in phosphoryl trichloride (10.6 mL, 115 mmol) and heated to 80° C. under nitrogen for 3 h. The reaction mixture was cooled to ambient temperature and poured into methyl tert-butyl ether (80 mL) with vigorous stirring. The mixture was stirred for 10 min and then filtered. The isolated solids were washed with methyl tert-butyl ether and dried in vacuum oven to afford the title compound (2.7 g), as a tan solid. After sitting for 2 d, the filtrate contained solids. The solids were isolated by filtration and dried to afford additional title compound (Total yield: 3.9 g, 90% yield).

4-Chloro-6-(1-(4-methoxybenzyl)-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

Step 1: Preparation of 4-Chloro-3-iodo-6-(1-(4-methoxybenzyl)-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine. Under a N_(2(g)) atmosphere, a mixture of 4-chloro-6-(1-(4-methoxybenzyl)-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine (10.0 g, 29.4 mmol) and NIS (7.95 g, 35.3 mmol) in DMF (200 mL) was stirred for 30 min at ambient temperature. Additional NIS (7.95 g, 35.3 mmol) was introduced as a solution in DMF (10 mL). The reaction mixture was stirred for 30 min at ambient temperature and then for 16 h at 50° C. before filtering the resultant suspension. The filter cake was rinsed with EtOAc (50 mL) and dried in a vacuum oven at 40° C. to afford the title compound (11.0 g, 80%). MS (apci) m/z=465.5 (M+H).

Step 2: Preparation of 4-Chloro-6-(1-(4-methoxybenzyl)-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile. Under a N_(2(g)) atmosphere, a cold (−19 to −25° C.) solution of 4-chloro-3-iodo-6-(1-(4-methoxybenzyl)-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine (2.0 g, 4.29 mmol) in THF (28 mL), was treated slowly with 1.68 M i-PrMgCl in THF (2.8 mL, 4.7 mmol), maintaining the internal temperature at or below −19° C. during the addition. The reaction was stirred for 20 min at −25° C., and then 1-cyanato-4-methoxybenzene (0.77 g, 5.15 mmol) was introduced as a solution in THF (2 mL), again maintaining the internal temperature at or below −19° C. during the addition. The reaction mixture was allowed to warm to 20° C. over 12 h, and then the resulting slurry was vacuum filtered. The isolated solids were purified by silica chromatography (stepped gradient eluent of 7:3, then 1:1, then 3:7 heptane-EtOAc) to afford the title compound (0.8 g, 52% yield). MS (apci) m/z=364.8 (M+H).

4-(6-Fluoropyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine

A mixture of 4-chloro-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine hydrochloride (Intermediate P1; 3.5 g, 13.0 mmol), (6-fluoropyridin-3-yl)boronic acid (2.28 g, 16.2 mmol), X-phos (1.24 g, 2.59 mmol), and Pd₂(dba)₃ (0.593 g, 0.648 mmol) in THF (40 mL) was sparged with Ar_((g)) for 30 seconds before adding 2 M K₂CO_(3(aq)) (19.4 mL, 38.9 mmol). The mixture was sparged with Ar_((g)) for an additional 5 min, then sealed, and stirred overnight at 70° C. The reaction mixture was diluted with DCM (250 mL) and saturated NaHCO_(3(aq)) (50 mL). This resulted in an emulsion which was resolved with the addition of 10% iPrOH in CHCl₃ (100 mL). The resultant biphasic mixture was separated, and the organic extracts were retained, while the aqueous extracts containing solid were washed with a mixture of DCM (3×250 mL) and 10% iPrOH in CHCl₃ (3×100 mL). All organic extracts were combined, then dried over anhydrous MgSO_(4(s)), filtered, and concentrated in vacuo. The residue was solubilized in DCM and MeOH, and purified by silica chromatography (using 60-75% EtOAc in DCM with 0.1% NH₄OH as the gradient eluent) to afford the title compound (0.800 g, 21% yield). MS (apci) m/z=295.1 (M+H). ¹H NMR (400 MHz, CDCl₃) δ: 8.95 (m, 1H), 8.56 (m, 1H), 8.50-8.54 (m, 1H), 8.06 (m, 1H), 7.94 (s, 2H), 7.11-7.14 (m, 1H), 6.92 (m, 1H), 3.98 (s, 3H).

3-Chloro-4-(6-fluoropyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine

A thick suspension of 4-(6-fluoropyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine (Intermediate P5; 0.523 g, 1.78 mmol) and NCS (0.237 g, 1.78 mmol) in DMF (20 mL) was stirred overnight at 50° C., then for another day at 60° C. Additional NCS (0.237 g, 1.78 mmol) was introduced, and the reaction was allowed to stir for 5 d at 60° C. The reaction mixture was quenched with water and vigorously stirred. The mixture was vacuum filtered. The filter cake was air dried overnight, then washed with Et₂O. The solids were dried in a vacuum oven for 2 d at 45° C., affording a mixture of the title compound and 4-(6-fluoropyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine (Intermediate P5) (0.554 g, ˜1:1 ratio by HPLC). This mixture was directly used in the next step without further purification.

4-(6-Fluoropyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

In a pressure vessel, 4-chloro-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile (Intermediate P2; 0.503 g, 1.94 mmol), 2-fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine (0.520 g, 2.33 mmol), and Pd(PPh₃)₄ (0.0674 g, 0.0583 mmol) were suspended in 2 M Na₂CO_(3(aq)) (5.83 mL, 11.7 mmol) and 1,4-dioxane (9.72 mL). The mixture was sparged with N_(2(g)) for 15 min, then sealed and stirred overnight at 80° C. The reaction mixture was cooled for 20 minutes before adding additional Pd(PPh₃)₄ (0.0674 g, 0.0583 mmol) and 2-fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine (0.075 g, 0.34 mmol) were introduced. The reaction mixture was sparged again with N_(2(g)) for 15 min, then sealed and stirred for 24 hrs at 80° C. The reaction mixture was cooled to room temperature, then poured into water (100 mL). The resulting suspension was filtered, and the filter cake was washed successively with water (2×5 mL) and Hexanes (2×5 mL). The solids were air dried to cleanly afford the title compound (0.44 g, 71% yield). MS (apci) m/z=320.1 (M+H).

6-bromo-4-(6-(4-((6-methoxypyridin-3-yl)methyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

A mixture of 4,6-dibromopyrazolo[1,5-a]pyrazine-3-carbonitrile (Intermediate R9; 153 mg, 0.507 mmol), 1-((6-methoxypyridin-3-yl)methyl)-4-(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)piperazine (Intermediate R1; 208 mg, 0.507 mmol), Cs₂CO_(3(s)) (330 mg, 1.01 mmol) and PdCl₂(dppf)⋅CH₂Cl₂ (41.4 mg, 0.0507 mmol) in 4:1 dioxane:water (1.5 mL) was sparged with N_(2(g)), then stirred overnight at ambient temperature. The reaction mixture was diluted with DCM and washed with saturated NaHCO_(3(aq)). The organic extracts were washed with brine, then dried over anhydrous Na₂SO_(4(s)), filtered, and concentrated in vacuo. The crude residue was purified by silica chromatography (using 1-9% DCM/MeOH with 1% NH₄OH as the gradient eluent) to cleanly afford the title compound (204 mg, 80% yield). MS (apci) m/z=505.1 (M+H).

1-((6-Methoxypyridin-3-yl)methyl)-4-(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)piperazine

A mixture of 1-(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)piperazine (5 g, 17.3 mmol) and 6-methoxynicotinaldehyde (2.85 g, 20.7 mmol) in DCE (85 mL) was treated portionwise with NaBH(AcO)₃ (7.3 g, 35 mmol). The mixture was stirred 2.5 h at ambient temperature, and then concentrated in vacuo to reduce the volume by half. The mixture was diluted with EtOAc, and washed sequentially with saturated NaHCO_(3(aq)) and brine. The organic extracts were dried over anhydrous Na₂SO_(4(s)), filtered, and concentrated in vacuo to afford the title compound (4.86 g, 69% yield). MS (apci) m/z=411.2 (M+H).

2-((tert-butoxycarbonyl)amino)-2-(2-fluorophenyl)acetic acid

A solution of 2-amino-2-(2-fluorophenyl)acetic acid (300 mg, 1.77 mmol) in THF (1.8 mL) was treated sequentially with 1 M NaOH_((aq)) (2.66 mL, 5.32 mmol) and di-tert-butyl dicarbonate (387 mg, 1.77 mmol). The resulting mixture was stirred overnight at ambient temperature before introducing additional di-tert-butyl dicarbonate (387 mg, 1.77 mmol). The reaction mixture was concentrated in vacuo. The residue was suspended in DCM, and washed sequentially with saturated NaHCO_(3(aq)), water and brine (2×2 mL each). The combined organic extracts were dried over anhydrous Na₂SO_(4(s)), filtered, and concentrated in vacuo. The residue was triturated with DCM/Hexanes (1:10) and dried under high vacuum to afford the title compound (486 mg, quantitative yield). MS (apci) m/z=268.1 (M+H)

2-((tert-butoxycarbonyl)amino)-2-(2,4-difluorophenyl)acetic acid

A solution of 2-amino-2-(2,4-difluorophenyl)acetic acid (300 mg, 1.60 mmol) in THF (1.6 mL) was treated sequentially with 2 M NaOH_((aq)) (2.41 mL, 4.81 mmol) and di-tert-butyl dicarbonate (385 mg, 1.76 mmol). After stirring the resulting mixture for 2 h at ambient temperature, additional di-tert-butyl dicarbonate (387 mg, 1.77 mmol) was introduced, and the reaction was stirred an additional 1.5 h. The reaction mixture was concentrated in vacuo. The residue was suspended in DCM and washed sequentially with saturated NaHCO_(3(aq)), water and brine (2×2 mL each). The combined organic extracts were dried over anhydrous Na₂SO_(4(s)), filtered, and concentrated in vacuo. The residue was triturated twice with DCM/Hexanes (1:10) and dried under high vacuum to afford the title compound (383 mg, 83% yield). MS (apci) m/z=286.1 (M−H)

2-((tert-butoxycarbonyl)amino)-2-(3-chloro-4-fluorophenyl)acetic acid

A solution of racemic 2-amino-2-(3-chloro-4-fluorophenyl)acetic acid (1 g, 4.9 mmol) in THF (50 mL) was treated sequentially with 2 M NaOH_((aq)) (7 mL, 15 mmol) and di-tert-butyl dicarbonate (1.18 g, 5.40 mmol). After stirring overnight at ambient temperature, the reaction mixture was concentrated in vacuo to approximately 10 mL. The concentrated mixture was neutralized with 1 M HCl_((aq)) (15 mL) then extracted with EtOAc (2×50 mL). The combined organic extracts were washed with brine (50 mL), dried over anhydrous MgSO_(4(s)), filtered, and concentrated in vacuo to afford the title compound (383 mg, 83% yield). MS (apci) m/z=301.9 (M+H).

(2S)-2-(1-(tert-butoxycarbonyl)pyrrolidin-2-yl)-2-phenylacetic acid

Step 1: Preparation of (R)-4-benzyl-3-(2-phenylacetyl)oxazolidin-2-one. A solution of (R)-(+)-4-Benzyl-2-oxazolidinone (2.80 g, 15.8 mmol) in THF (100 mL) was cooled to −78° C., then treated with 1M [(CH₃)₃Si]₂NLi in THF (15.8 mL, 15.8 mmol). The reaction mixture was stirred at −78° C. for 15 min before treating with (R)-(+)-4-benzyl-2-oxazolidinone (2.80 g, 15.8 mmol). After allowing the resulting mixture to slowly warm to ambient temperature over 2 h, the reaction mixture was stirred for an additional 60 h at ambient temperature. The reaction mixture was treated with saturated NaHCO_(3(aq)) then extracted with EtOAc (2×). The combined organic extracts were extracted with water (3×) and brine (1×), and then dried over anhydrous Na₂SO_(4(s)), filtered, and concentrated in vacuo. The residue was purified by silica chromatography (using 5-60% Hexanes-EtOAc as the gradient eluent) to afford the title compound (3.53 g, 79% yield). 1H NMR (400 MHz, DMSO-d₆) δ 7.36-7.12 (m, 10H), 4.70-4.65 (m, 1H), 4.36-4.11 (m, 4H), 3.01-2.88 (m, 2H).

Step 2: Preparation of tert-butyl 2-((S)-2-((R)-4-benzyl-2-oxooxazolidin-3-yl)-2-oxo-1-phenylethyl)pyrrolidine-1-carboxylate. A solution of (R)-4-benzyl-3-(2-phenylacetyl)oxazolidin-2-one (Step 1; 1.11 g, 3.76 mmol) in DCM (38 mL) was cooled to −78° C., and then sequentially treated with DIEA (786 μL, 4.51 mmol) and TiCl₄ (495 μL, 4.51 mmol). After stirring at −78° C. for 30 min, tert-butyl 2-methoxypyrrolidine-1-carboxylate (1.14 g, 5.64 mmol) was introduced. The cooling bath was removed, and the reaction mixture was stirred 16 h at ambient temperature. The reaction mixture then was cooled to 0° C., quenched with saturated NaHCO_(3(aq)) and stirred at 0° C. for 15 min. The quenched mixture was extracted with EtOAc (2×), and the combined organic extracts were washed with water (2×) and brine (1×). The organic extracts were dried over anhydrous Na₂SO_(4(s)), filtered, and concentrated in vacuo. The residue was purified by silica chromatography (using 5-60% Hexanes-EtOAc as the gradient eluent) to afford the title compound (374.5 mg, 21% yield). MS (apci) m/z=365.2 (M+H−Boc).

Step 3: Preparation of (2S)-2-(1-(tert-butoxycarbonyl)pyrrolidin-2-yl)-2-phenylacetic acid. A solution of 1 M LiOH_((aq)) (806.1 μL, 1.612 mmol) in 1:1 THF:water (4.0 mL) was cooled to 0° C. The resulting cold solution was treated with 32 wt % H₂O_(2 (aq)) (205.9 μL, 2.015 mmol). After stirring at 0° C. for 15 min, tert-butyl 2-((S)-2-((R)-4-benzyl-2-oxooxazolidin-3-yl)-2-oxo-1-phenylethyl)pyrrolidine-1-carboxylate (Step 2; 374.5 mg, 0.8061 mmol) was introduced. The resulting mixture was stirred 16 h at ambient temperature. The reaction mixture was quenched with 10% Na₂S₂O_(3(aq)), diluted with Et₂O and washed with 1 M NaOH_((aq)) (2×). The combined aqueous extracts were back extracted with Et₂O (2×). The aqueous extracts were acidified to pH 4 using 4 M HCl_((aq)) and extracted with 4:1 DCM:iPrOH (2×). The combined DCM:iPrOH extracts were dried over anhydrous Na₂SO_(4(s)), filtered, and concentrated in vacuo to afford the title compound (246.2 mg, quantitative yield). MS (apci) m/z=206.2 (M+H−Boc).

3-methyl-6-(piperidin-4-yloxy)pyridazine

Step 1: Preparation of tert-butyl 4-((6-methylpyridazin-3-yl)oxy)piperidine-1-carboxylate. A solution of tert-butyl 4-hydroxypiperidine-1-carboxylate (10.22 g, 50.75 mmol) in DMF (56.39 mL) was treated with 60% w/w NaH (2.165 g, 54.14 mmol) at ambient temperature and allowed to stir for 10 min. The reaction mixture was treated with 3-chloro-6-methylpyridazine (4.350 g, 33.84 mmol). The reaction mixture was stirred for 10 min at ambient temperature and then at 90° C. for 48 h. The reaction mixture was cooled to ambient temperature and quenched with saturated NaHCO_(3(aq)) (20 mL) and water (20 mL). The quenched mixture was extracted with DCM (3×40 mL), and the combined organic extracts were washed with water (3×100 mL) and brine (3×100 mL). The combined organic extracts were dried over anhydrous Na₂SO_(4(s)), filtered, and concentrated in vacuo to afford the title compound (quantitative yield assumed). MS (apci) m/z=294.20 (M+H).

Step 2: Preparation of 3-methyl-6-(piperidin-4-yloxy)pyridazine. A solution of tert-butyl 4-((6-methylpyridazin-3-yl)oxy)piperidine-1-carboxylate (Step 1; 9.93 g, 33.8 mmol) in DCM (10.9 mL) was treated with TFA (13.0 mL, 169 mmol). After stirring for 20 min at ambient temperature, the reaction mixture was treated with additional TFA (13 mL). The reaction mixture was stirred for an additional 1.5 h at ambient temperature before concentrating the mixture in vacuo. The residue was purified by silica chromatography (using 1-9% MeOH in DCM with 0.1% NH₄OH as the gradient eluent). The fractions containing the desired product were combined and concentrated in vacuo. The residue was triturated with DCM (10 mL) and Hexanes (20 mL) and then concentrated in vacuo to afford the title compound (5.51 g, 84% yield). MS (apci) m/z=194.2 (M+H).

3-methoxy-6-(piperidin-4-yloxy)pyridazine

Step 1: Preparation of tert-butyl 4-((6-methoxypyridazin-3-yl)oxy)piperidine-1-carboxylate. A room temperature solution of tert-butyl 4-hydroxypiperidine-1-carboxylate (2.0 g, 9.94 mmol) in DMF (16.6 mL) was treated with 60% w/w NaH (0.437 g, 10.9 mmol). After stirring for 15 min at ambient temperature, reaction mixture was treated with 3-chloro-6-methoxypyridazine (1.44 g, 9.94 mmol). The resulting mixture was stirred for 15 min at ambient temperature then overnight at 90° C. The reaction was incomplete at this point, therefore, the reaction mixture was cooled to 0° C., and treated with additional 60% w/w NaH (0.437 g, 10.9 mmol) and tert-butyl 4-hydroxypiperidine-1-carboxylate (2.0 g, 9.94 mmol) The resulting mixture was stirred for 15 min at 0° C., then brought to ambient temperature and finally heated at 90° C. for an additional 24 h. This process of cooling the reaction to introduce supplemental reagent was repeated once more before the reaction mixture was quenched at ambient temperature with the addition of saturated NaHCO_(3(aq)) (4 mL) and water (4 mL). The quenched mixture was extracted with EtOAc (3×8 mL), and the combined organic extracts were washed with water (3×20 mL) and brine (1×20 mL). The organic extracts were dried over anhydrous Na₂SO_(4(s)), filtered, and concentrated in vacuo. The crude residue was purified by silica chromatography (using 5-50% EtOAc in Hexanes as the gradient eluent) to afford title compound (1.57 g, 51% yield). MS (apci) m/z=310.20 (M+H).

Step 2: Preparation of 3-methoxy-6-(piperidin-4-yloxy)pyridazine. A solution of tert-butyl 4-((6-methoxypyridazin-3-yl)oxy)piperidine-1-carboxylate (Step 1; 0.706 g, 2.28 mmol) in DCM (0.734 mL) was treated with TFA (0.879 mL, 11.4 mmol). After stirring for 15 min at ambient temperature, the reaction mixture concentrated in vacuo. The residue was purified by silica chromatography (using 1-9% MeOH in DCM with 0.1% NH₄OH as the gradient eluent) to afford the title compound (0.390 g, 82% yield). MS (apci) m/z=210.1 (M+H).

N-(3-methylpiperidin-3-yl)acetamide 2,2,2-trifluoroacetate

Step 1: Preparation of tert-butyl 3-acetamido-3-methylpiperidine-1-carboxylate. A solution of tert-butyl 3-amino-3-methylpiperidine-1-carboxylate (0.1091 g, 0.5091 mmol) and TEA (0.1419 mL, 1.018 mmol) in DCM (5.1 mL) was treated with acetic anhydride (72.05 μL, 0.7636 mmol). The reaction was monitored for completion by TLC (EtOAc/silica, using ninhydrin stain). Upon completion, the reaction mixture was diluted with DCM (40 mL) and washed with brine (3×20 mL). The organic extracts were dried over anhydrous MgSO_(4(s)), filtered, and concentrated in vacuo. The crude residue was purified by silica chromatography using DCM as eluent to afford title compound (0.104 g, 80% yield). MS (apci) m/z=157.2 (M+H−Boc).

Step 2: Preparation of N-(3-methylpiperidin-3-yl)acetamide 2,2,2-trifluoroacetate. A solution of tert-butyl 3-acetamido-3-methylpiperidine-1-carboxylate (Step 1; 0.104 g, 0.407 mmol) in CHCl₃ (0.734 mL) was treated with TFA (1.6 mL, 20 mmol). The reaction was monitored for completion by TLC (EtOAc/silica, using ninhydrin stain). Upon completion the reaction mixture was concentrated in vacuo to afford the title compound (112 mg, quantitative yield). MS=157.2 (M+H−BOC).

4,6-dibromopyrazolo[1,5-a]pyrazine-3-carbonitrile

Step 1: Preparation of 1-amino-3,5-dibromopyrazin-1-ium 2,4,6-trimethylbenzenesulfonate. Under an inert atmosphere (N_(2(g))) a cold (0° C.) solution of O-(mesitylsulfonyl)hydroxylamine (Intermediate R10; 9.8 g, 45 mmol) in DCM (300 mL) was treated portion-wise with 2,6-dibromopyrazine (9.0 g, 38 mmol). The resulting mixture was stirred for 48 h at ambient temperature and concentrated to minimal DCM to provide the title compound (17 g, 99% yield) which was used crude in the next step. MS (apci) m/z=235.9.2 (M+H).

Step 2: Preparation of 4,6-dibromopyrazolo[1,5-a]pyrazine-3-carbonitrile. The DCM slurry of 1-amino-3,5-dibromopyrazin-1-ium 2,4,6-trimethylbenzenesulfonate (Step 1; 17 g, 37.5 mmol) was diluted with 1,4-dioxane (200 mL) then treated with acrylonitrile (5.65 mL, 86.3 mmol) and DIEA (8.52 mL, 48.8 mmol). After stirring the resulting mixture for 3 h at ambient temperature, 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) (17.9 g, 78.8 mmol) was added, and the reaction was stirred for an additional 3 h at ambient temperature. The reaction mixture was extracted with EtOAc (500 mL) and water (400 mL). The organic extracts were treated with silica gel (40 g). The resulting slurry was concentrated in vacuo, then loaded on top of a silica gel plug (200 g) and rinsed with 20% ethyl acetate/hexanes. The filtrate was concentrated in vacuo and purified by silica chromatography (using 10-40% EtOAc/Hexanes as the gradient eluent) to cleanly afford the title compound (2.3 g, 20% yield). 1H NMR (400 MHz, DMSO-d₆) δ 9.60 (s, 1H), 8.91 (s, 1H).

O-(mesitylsulfonyl)hydroxylamine

Step 1: Preparation of tert-butyl (mesitylsulfonyl)oxycarbamate. To a 0° C. solution of 2,4,6-trimethylbenzene-1-sulfonyl chloride (10.0 g, 45.72 mmol) and tert-butyl hydroxycarbamate (6.088 g, 45.72 mmol) in MTBE (100 mL) was added TEA (14.46 mL, 48.01 mmol) drop-wise while stirring. The resulting suspension was stirred at 0° C. for an additional 30 min and then warmed to ambient temperature. The reaction was diluted with water (100 mL), adjusted to pH 4 with 1 N HCl_((aq)). The organic layer was dried (Na₂SO₄), filtered and concentrated to yield the title compound initially as a yellowish oil, which upon drying overnight under high vacuum became a white solid (12.89 g, 89% yield). 1H NMR (CDCl₃) δ 7.66 (br s, 1H), 6.98 (s, 2H), 2.67 (s, 6H), 2.32 (s, 3H), 1.31 (s, 9H).

Step 2: Preparation of O-(mesitylsulfonyl)hydroxylamine (Intermediate R1, MSH). To TFA (117 mL, 1521 mmol) at 0° C. was slowly added tert-butyl (mesitylsulfonyl)oxycarbamate (39.0 g, 124 mmol) over 25 min. The reaction mixture was stirred at 0° C. for 1.5 h and then quenched with the sequential addition of crushed ice (5×200 mL) and water (2×125 mL). The resulting thick suspension was vigorously stirred at ambient temperature for 5 min. Without allowing the filter cake to run dry, the solids were collected by careful vacuum filtration followed by subsequent rinsing with water (4 L) until the filtrate reached pH 6 (Caution: explosion risk exists with dry compound at ambient temperature). The wet filter cake was taken up in DCM (150 mL) and the resulting biphasic solution was separated. The DCM layer was dried over MgSO₄ for 30 min and then filtered and rinsed with DCM (420 mL) to provide the title compound as a 0.22 M solution in DCM.

(6-(6-(tert-butoxycarbonyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)boronic acid

Method 1:

Step 1: Preparation of tert-butyl 3-(5-bromopyridin-2-yl)-3,6-diazabicyclo[3.1.1]heptane-6-carboxylate. A suspension of 3,6-diaza-bicyclo[3.1.1]heptane-6-carboxylic acid tert-butyl ester (1.046 g, 5.27 mmol), 5-bromo-2-fluoropyridine (919 mg, 5.22 mmol) and K₂CO_(3(s)) (3.61 g, 26.1 mmol) in DMSO (5.22 mL) was stirred for 1 day at 90° C. After cooling to ambient temperature, the reaction mixture was partitioned between EtOAc and water. The organic extracts were washed with additional water, then dried over anhydrous Na₂SO_(4(s)), filtered, and concentrated in vacuo. Purification of the crude residue by silica chromatography (0-50% Hexanes/EtOAc as gradient eluent) provided the title compound (1.80 g, 97% yield). MS (apci) m/z=354.0 (M+1), 356.1 (M+2).

Step 2: Preparation of (6-(6-(tert-butoxycarbonyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)boronic acid. A mixture of tert-butyl 3-(5-bromopyridin-2-yl)-3,6-diazabicyclo[3.1.1]heptane-6-carboxylate (1.80 g, 5.08 mmol), bis(pinacolato)diboron (3.87 g, 15.2 mmol), PdCl₂(dppf)⋅CH₂Cl₂ (414 mg, 0.508 mmol), and KOAc (1.50 g, 15.2 mmol) in dioxane (5.75 mL) was sparged with N_(2(g)), then stirred for 3 h at 80° C. After cooling to room temperature, the reaction mixture was diluted with DCM and washed with water. The aqueous extracts were washed with DCM. The DCM extracts were combined and dried over anhydrous Na₂SO_(4(s)), filtered, and concentrated in vacuo. The crude residue was sonicated with hexanes (200 mL) and ether (50 mL) for 5 min, and the resulting gray suspension was filtered. The collected solids were triturated with MeOH, and the resulting suspension was filtered to afford the title compound as a white solid (840 mg, 52% yield). MS (apci) m/z=320.2 (M+H).

Method 2:

A suspension of 3,6-diaza-bicyclo[3.1.1]heptane-6-carboxylic acid tert-butyl ester (182 mg, 0.918 mmol), 2-fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine (819 mg, 3.67 mmol) and K₂CO_(3(s)) (634 mg, 4.59 mmol) in DMSO (918 μL) was heated to 90° C., then treated with water (5 mL). The resulting mixture was stirred for 1 hour at 90° C., then cooled to ambient temperature and filtered to cleanly provide the title compound (1.0 g, 41% yield). MS (apci) m/z=320.1 (M+H).

Preparation of Synthetic Examples Example 1

3,3-Dimethyl-1-(4-(4-(6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)phenyl)piperazin-1-yl)butan-1-one

Step 1: Preparation of tert-Butyl 4-(5-(6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperazine-1-carboxylate and tert-Butyl 4-(5-(3-chloro-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperazine-1-carboxylate. A mixture (1:1) of 4-(6-fluoropyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine (Intermediate P5; 242 mg, 0.821 mmol), 3-chloro-4-(6-fluoropyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine (Intermediate P6; 900 mg, 0.821 mmol) and tert-butyl piperazine-1-carboxylate (1530 mg, 8.213 mmol) in dioxane (5 mL) was stirred for 2 d at 90° C. The reaction was cooled to ambient temperature, then diluted with saturated NH₄Cl_((aq)) (20 mL) and brine (2 mL). The mixture was extracted with EtOAc (3×), and the combined organic extracts were concentrated in vacuo. The residue was purified by C18 reverse phase chromatography (using 0-70% ACN/water as the gradient eluent) to cleanly isolate tert-Butyl 4-(5-(3-chloro-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperazine-1-carboxylate (102 mg, 25% yield), MS (apci) m/z=495.0 (M+H), 497.1, (M+H+2) with Cl pattern, as well as a mixture (1:1) of the both title compounds (130 mg, 34% yield), MS (apci) m/z=461.1 (M+H).

Step 2: Preparation of 3,3-Dimethyl-1-(4-(4-(6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)phenyl)piperazin-1-yl)butan-1-one. A mixture (1:1) of tert-butyl 4-(5-(6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperazine-1-carboxylate and tert-butyl 4-(5-(3-chloro-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperazine-1-carboxylate (130 mg, 0.282 mmol) in DCM (10 mL) was treated with 5 M HCl in iPrOH (135 μL, 0.67 mmol). The mixture was stirred overnight at ambient temperature then concentrated in vacuo to afford the crude product as a mixture (1:1) of 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine dihydrochloride and 3-chloro-6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine dihydrochloride. A portion of this crude product mixture (40 mg, 0.10 mmol) in DMF (0.5 mL) was treated sequentially with 3,3-dimethylbutanoyl chloride (41 mg, 0.30 mmol) and TEA (70 μL, 0.50 mmol). The mixture was stirred for 4 h at ambient temperature, then directly purified by C18 reverse phase chromatography (using 0-70% ACN/water as the gradient eluent) to separately afford the title compound, 3,3-dimethyl-1-(4-(4-(6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)phenyl)piperazin-1-yl)butan-1-one (6.5 mg, 28% yield), MS (apci) m/z=459.1 (M+H). In addition, compound 1-(4-(4-(3-chloro-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)phenyl)piperazin-1-yl)-3,3-dimethylbutan-1-one (Example 2; 8.9 mg, 36% yield) was also isolated during chromatography purification.

Example 2

1-(4-(4-(3-Chloro-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)phenyl)piperazin-1-yl)-3,3-dimethylbutan-1-one

The title compound was isolated during the preparation of Example 1. MS (apci) m/z=493.1 (M+H), 495.1 (M+H+2) with Cl pattern.

Examples 3 1-(4-(5-(3-Chloro-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperazin-1-yl)ethan-1-one

A mixture (1:1) of 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine dihydrochloride and 3-chloro-6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine dihydrochloride (Example 1; Step 2; 33 mg, 0.083 mmol) in DMF (0.5 mL) was treated sequentially with acetyl chloride (249 μL, 0.25 mmol) and TEA (58 μL, 0.42 mmol). The mixture was stirred for 2 h at ambient temperature then directly purified by C18 reverse phase chromatography (using 0-70% ACN/water as the gradient eluent) to separately afford the title compound (8 mg, 44% yield). MS (apci) m/z=437.0 (M+H), 439.1 (M+H+2).

Example 4

1-(4-(5-(3-Chloro-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperazin-1-yl)-2-(dimethylamino)ethan-1-one

Step 1: Preparation of 3-Chloro-6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine dihydrochloride. A solution of 4-(5-(3-chloro-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperazine-1-carboxylate (Example 1, Step 1; 202 mg, 0.408 mmol) in DCM (10 mL) was treated with 5 M HCl in iPrOH (408 μL, 2.04 mmol). The mixture was stirred overnight at ambient temperature then concentrated in vacuo to afford the title compound (177 mg, quantitative yield). MS (apci) m/z=395.0 (M+H), 397.0 (M+H+2) with Cl pattern.

Step 2: Preparation of 1-(4-(5-(3-Chloro-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperazin-1-yl)-2-(dimethylamino)ethan-1-one. A solution of 3-chloro-6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine dihydrochloride (30 mg, 0.070 mmol) in DMF (0.5 mL) was treated sequentially with 2-(dimethylamino)acetyl chloride (25 mg, 0.21 mmol) and TEA (48 μL, 0.35 mmol). The mixture was stirred for 2 h at ambient temperature then directly purified by C18 reverse phase chromatography (using 0-70% ACN/water as the gradient eluent) to afford the title compound (26 mg, 78% yield). MS (apci) m/z=480.1 (M+H), 481.1 (M+H+2) with Cl pattern.

Example 5

4-(6-(4-Benzylpiperazin-1-yl)pyridin-3-yl)-3-chloro-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine

A solution of 3-chloro-6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine dihydrochloride, contaminated with 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine dihydrochloride (Example 4, Step 1; 20 mg, 0.043 mmol) in DMF (0.2 mL) was treated with (bromomethyl)benzene (11 mg, 0.064 mmol) and TEA (18 μL, 0.13 mmol). The reaction mixture was allowed to stir for 1 h at ambient temperature, and then directly purified by C18 reverse phase chromatography (using 0-60% ACN/water as the gradient eluent) to afford the title compound (2.9 mg, 14% yield). MS (apci) m/z=485.1 (M+H), 487.1 (M+H+2) with Cl pattern.

Example 6

3-Chloro-6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(4-(pyridin-2-ylmethyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine

A solution of 3-chloro-6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine dihydrochloride, contaminated with 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine dihydrochloride (Example 4, Step 1; 18.5 mg, 0.0428 mmol in DMF (0.2 mL) was treated with picolinaldehyde (6.87 mg, 0.0641 mmol), Me₄N(AcO)₃BH (22.5 mg, 0.0855 mmol) and TEA (17.9 μL, 0.128 mmol). The reaction mixture was allowed to stir overnight at ambient temperature and then directly purified by C18 reverse phase chromatography (using 0-60% ACN/water as the gradient eluent) to afford the title compound (14.8 mg, 71% yield). MS (apci) m/z=486.1 (M+H), 487.1 (M+H+2) with Cl pattern.

Example 7 tert-Butyl 4-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperazine-1-carboxylate

In a pressure vessel, a mixture of 4-chloro-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile (Intermediate P2; 2.85 g, 11.0 mmol) and tert-butyl 4-(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)piperazine-1-carboxylate (6.43 g, 16.5 mmol) in 1,4-dioxane (44.1 mL) and 2 N K₂CO_(3(aq)) (33.1 mL, 66.1 mmol) was sparged with N_(2(g)) for 5 min. The mixture was treated with Pd(PPh₃)₄ (0.0674 g, 0.0583 mmol), then sealed and stirred 30 h at 90° C. After cooling to ambient temperature, the resultant biphasic suspension was vacuum filtered, and the filter cake was rinsed sequentially with 2 N K₂CO_(3(aq)) (ca. 20 mL) and water (3×20 mL). The solids were air dried for 4 h, then dried under high vacuum overnight to cleanly afford the title compound (5.94 g, quantitative yield). MS (apci) m/z=486.2 (M+H).

Example 8

6-(1-Methyl-1H-pyrazol-4-yl)-4-(6-(piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile dihydrochloride

A mixture of tert-butyl 4-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperazine-1-carboxylate (Example 7; 433 mg, 0.892 mmol) and TFA (687 μL, 8.92 mmol) in DCM (10 mL) was stirred for 90 min at ambient temperature, then concentrated in vacuo. The residue was purified by silica chromatography (using 0-10% CHCl₃/MeOH with 0.1% NH₄OH as the gradient eluent to afford the title compound (384 mg, quantitative yield). MS (apci) m/z=386.2 (M+H−Boc).

Example 9

6-(1-Methyl-1H-pyrazol-4-yl)-4-(6-(4-(3-methylbutanoyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

A solution of 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile dihydrochloride (Example 8; 15 mg, 0.039 mmol) in DCM (2 mL) was treated sequentially with 3-methylbutanoyl chloride (7.0 mg, 0.058 mmol) and TEA (54 μL, 0.39 mmol). The mixture was stirred overnight at ambient temperature, then quenched with water and extracted with DCM (3×) in a PS frit. The combined organic extracts were concentrated in vacuo, and the residue was purified by C18 reverse phase chromatography (using 0-70% ACN/water as the gradient eluent) to afford the title compound (12 mg, 66% yield). MS (apci) m/z=470.1 (M+H).

Example 10

6-(1-Methyl-1H-pyrazol-4-yl)-4-(6-(4-(2-(tetrahydro-2H-pyran-4-yl)acetyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

A solution of 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile dihydrochloride (Example 8; 10 mg, 0.026 mmol) in DCM (2 mL) was treated sequentially with 2-(tetrahydro-2H-pyran-4-yl)acetyl chloride (6.3 mg, 0.039 mmol) and TEA (36 μL, 0.26 mmol). The mixture was stirred overnight at ambient temperature, then quenched with water, and extracted with DCM (3×) in a PS frit. The combined organic extracts were concentrated in vacuo, and the residue was purified by C18 reverse phase chromatography (using 0-70% ACN/water as the gradient eluent) to afford the title compound (2.6 mg, 20% yield). MS (apci) m/z=512.2 (M+H).

Example 11

6-(1-Methyl-1H-pyrazol-4-yl)-4-(6-(4-(quinoxaline-6-carbonyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

A solution of 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile dihydrochloride (Example 8; 30 mg, 0.078 mmol), 6-quinoxalinecarbonyl chloride (30 mg, 0.16 mmol) and DIEA (68 μL, 0.39 mmol) in DMF (156 μL) was stirred overnight at ambient temperature. The mixture was partitioned between EtOAc and water. The aqueous extracts were extracted with EtOAc (3×). The combined organic extracts were washed with brine (1×), then dried over anhydrous Na₂SO_(4(s)), filtered, and concentrated in vacuo. The residue was purified by C18 reverse phase chromatography (using 5-95% ACN/water with 0.1% TFA as the gradient eluent) to provide the TFA salt of the title compound. The TFA salt was treated with saturated NaHCO_(3(aq)), and extracted into EtOAc (2×). The combined organic extracts were dried over anhydrous Na₂SO_(4(s)), filtered, and concentrated in vacuo to afford the title compound (1.0 mg, 2.4% yield). MS (apci) m/z=542.2 (M+H).

Example 12

(R)-4-(6-(4-(2-Hydroxy-2-phenylacetyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

A solution of 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile dihydrochloride (Example 8; 10 mg, 0.026 mmol) in DCM (2 mL) was treated sequentially with (R)-2-hydroxy-2-phenylacetic acid (5.0 mg, 0.033 mmol), TEA (30 μL, 0.22 mmol) and HATU (8.3 mg, 0.022 mmol). The mixture was stirred 1 h at ambient temperature before concentrating in vacuo. The residue was purified by C18 reverse phase chromatography (using 0-75% ACN/water as the gradient eluent) to afford the title compound (3.0 mg, 26% yield). MS (apci) m/z=520.1 (M+H).

Example 13

(R)-4-(6-(4-(2-Hydroxy-3-methylbutanoyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

The title compound (2.2 mg, 21% yield) was prepared and purified using a similar procedure to that described for Example 12, replacing (R)-2-hydroxy-2-phenylacetic acid with (R)-2-hydroxy-3-methylbutanoic acid, and replacing the DCM with DMF. MS (apci) m/z=520.1 (M+H).

Example 14

4-(6-(4-(3-(5-Fluoropyridin-2-yl)acetyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

A solution of 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile dihydrochloride (Example 8; 30 mg, 0.078 mmol) in DCM (1 mL) was treated sequentially with DIEA (27 μL, 0.16 mmol), 2-(5-fluoropyridin-2-yl)acetic acid (14 mg, 0.093 mmol) and HATU (30 mg, 0.078 mmol). The mixture was stirred overnight at ambient temperature before concentrating in vacuo. The residue was purified by C18 reverse phase chromatography (using 5-95% ACN/water with 0.1% TFA as the gradient eluent) to provide the TFA salt of the title compound. The TFA salt was treated with saturated NaHCO_(3(aq)), and subsequently extracted into DCM. The combined organic extracts were dried over anhydrous Na₂SO_(4(s)), filtered, and concentrated in vacuo. The residue was further purified by silica chromatography (using 0-20% MeOH in DCM as the gradient eluent) to cleanly afford the title compound (2.6 mg, 6.2% yield). MS (apci) m/z=522.8 (M+H).

Example 15

4-(6-(4-(2-Isopropoxyacetyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

A suspension of 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile dihydrochloride (Example 8; 20 mg, 0.0436 mmol) in anhydrous DMA (0.4 mL) was treated sequentially with DIEA (22.7 μL, 0.131 mmol), HATU (24.9 mg, 0.0655 mmol) and 2-isopropoxyacetic acid (7.73 mg, 0.0655 mmol). The mixture was stirred overnight at ambient temperature. Additional DIEA (15 μL, 0.087 mmol) and HATU (15 mg, 0.040 mmol) were added twice over a period of 24 h while stirring at ambient temperature. The reaction mixture was quenched with the addition of water in CHCl₃. The quenched mixture was stirred 30 min at room temperature, then extracted with CHCl₃ (3×) in a PS frit. The combined organic extracts were concentrated in vacuo, and the residue was purified by C18 reverse phase chromatography (using 15-80% ACN/water as the gradient eluent) to cleanly afford the title compound (3.6 mg, 17% yield). MS (apci) m/z=486.2 (M+H).

The compounds in Table A were prepared using a similar method to that described for the synthesis of Example 15, replacing 2-isopropoxyacetic acid with the appropriate carboxylic acid. Reactions were monitored for completion by LCMS, and reaction durations, along with the timing (and quantities) of the introduction of additional DIEA and HATU, were adjusted accordingly. In all cases reactions were quenched with water and CHCl₃ or DCM, and title compounds were cleanly isolated following C18 reverse phase chromatography using an appropriate gradient.

TABLE A MS (apci) Ex # Structure Chemical Name m/z 16

4-(6-(4-(1- (methoxymethyl)cyclo propane-1- carbonyl)piperazin-1- yl)pyridin-3-yl)-6-(1- methyl-1H-pyrazol-4- yl)pyrazolo[1,5- a]pyrazine-3- carbonitrile 498.2 (M + H) 17

4-(6-(4-(2- isopropoxypropanoyl) piperazin-1-yl)pyridin- 3-yl)-6-(1-methyl-1H- pyrazol-4- yl)pyrazolo[1,5- a]pyrazine-3- carbonitrile 500.2 (M + H)

Example 18

4-(5-(3-Cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)-N-isobutylpiperazine-1-carboxamide

A suspension of 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile dihydrochloride (Example 8; 0.101 g, 0.220 mmol) in anhydrous DMA (3 mL) was treated with TEA (0.154 mL, 1.10 mmol) and 1-isocyanato-2-methylpropane (0.0262 g, 0.264 mmol). The mixture was stirred for 4 h at ambient temperature before an additional drop of 1-isocyanato-2-methylpropane was added. The reaction mixture was stirred for an additional 2 hrs at ambient temperature before directly purifying by C18 reverse phase chromatography (using 20-80% ACN/water with 0.1% formic acid as the gradient eluent) to cleanly afford the title compound (50 mg, 47% yield). MS (apci) m/z=485.2 (M+H).

Example 19

(R)-4-(5-(3-Cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)-N-(1-(4-fluorophenyl)ethyl)piperazine-1-carboxamide

The title compound (24.2 mg, 59% yield) was prepared and purified using a similar procedure to that described for Example 18, replacing 1-isocyanato-2-methylpropane with (R)-1-fluoro-4-(1-isocyanatoethyl)benzene. As the reaction was monitored for completion by LCMS, the addition of supplemental isocyanate was omitted, and the reaction was complete within 6 hrs. MS (apci) m/z=550.2 (M+H).

Example 20

6-(1-Methyl-1H-pyrazol-4-yl)-4-(6-(4-(pyrrolidine-1-carbonyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

A suspension of 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile dihydrochloride (Example 8; 20 mg, 0.044 mmol) and DIEA (38 μL, 0.22 mmol) in DCM (218 μL) was treated with pyrrolidine-1-carbonyl chloride (6.4 mg, 0.048 mmol). The reaction mixture was stirred overnight at ambient temperature, then concentrated in vacuo. The residue was purified by C18 reverse phase chromatography (using 5-95% ACN/water with 0.1% TFA as the gradient eluent) to provide the TFA salt of the title compound. The TFA salt was treated with saturated NaHCO_(3(aq)), and subsequently extracted into EtOAc. The combined organic extracts were dried over anhydrous Na₂SO_(4(s)), filtered, and concentrated in vacuo. The residue was further purified by silica chromatography (using 0-20% MeOH in EtOAc as the gradient eluent) to cleanly afford the title compound (2.6 mg, 12% yield). MS (apci) m/z=483.2 (M+H).

Example 21

(S)-4-(6-(4-(3-Methoxypyrrolidine-1-carbonyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

Step 1: Preparation of 4-Nitrophenyl 4-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperazine-1-carboxylate. A suspension of 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile dihydrochloride (Example 8; 100 mg, 0.218 mmol) in DMA (2.18 mL) was treated sequentially with DIEA (114 μL, 0.655 mmol) and 4-nitrophenyl carbonochloridate (48.4 mg, 0.240 mmol). The reaction mixture was stirred 6 h at ambient temperature before introducing additional 4-nitrophenyl carbonochloridate (22 mg, 0.109 mmol). The resultant mixture was stirred 2 h at ambient temperature. LCMS analysis of the mixture indicated clean conversion to the title compound (120 mg, quantitative yield is assumed). MS (apci) m/z=551.2 (M+H). The mixture was divided into 5 equal parts for immediate use in subsequent reactions.

Step 2: Preparation of (S)-4-(6-(4-(3-Methoxypyrrolidine-1-carbonyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile. A solution of (S)-3-methoxypyrrolidine (5.5 mg, 0.054 mmol) and DIEA (19 μL, 0.11 mmol) in DMA (0.1 mL) was treated with a suspension 4-nitrophenyl 4-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperazine-1-carboxylate (Example 21, Step 1; 20 mg, 0.036 mmol) in DIEA (23 μL, 0.13 mmol) and DMA (0.44 mL). The reaction mixture was stirred overnight at 80° C. After cooling to ambient temperature, the reaction mixture was diluted with water and extracted with EtOAc (3×). The combined organic extracts were dried over anhydrous Na₂SO_(4(s)), filtered, and concentrated in vacuo. The residue was purified by C18 reverse phase chromatography (using 5-95% ACN/water with 0.1% TFA as the gradient eluent) to provide the TFA salt of the title compound. The TFA salt was treated with saturated NaHCO_(3(aq)) and extracted into EtOAc (3×). The combined organic extracts were concentrated in vacuo, and the residue was purified by silica chromatography (using 0-100% (20% MeOH/2% NH₄OH/78% DCM) in DCM as the gradient eluent) to cleanly afford the title compound (5.6 mg, 29% yield). MS (apci) m/z=513.2 (M+H).

Example 22

(S)-4-(6-(4-(3-Fluoropyrrolidine-1-carbonyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

The title compound was prepared and purified using a similar procedure to that described for Example 21, replacing (S)-3-methoxypyrrolidine with (S)-3-fluoropyrrolidine. The reaction was monitored for completion by LCMS. Additional (S)-3-fluoropyrrolidine (4.9 mg, 0.054 mmol) was introduced, and the reaction duration was adjusted to ensure reaction completion. Additionally, the gradient eluent in the final silica chromatography was altered (0-20% MeOH in DCM) to allow clean isolation of the title compound (1 mg, 6% yield) MS (apci) m/z=501.2 (M+H).

Example 23

6-(1-Methyl-1H-pyrazol-4-yl)-4-(6-(4-(2-(phenylsulfonyl)ethyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

A suspension of 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile dihydrochloride (Example 8; 21 mg, 0.046 mmol) in anhydrous DMA (0.5 mL) was treated with TEA (46.4 μL, 0.458 mmol) and ((2-chloroethyl)sulfonyl)benzene (28.1 mg, 0.137 mmol). The mixture was stirred overnight at 75° C. before cooling to ambient temperature. The reaction mixture was purified directly by C18 reverse phase chromatography (using 20-80% ACN/water as the gradient eluent) to cleanly afford the title compound (3.7 mg, 15% yield). MS (apci) m/z=554.2 (M+H).

The compounds in Table B were prepared using a similar method to that described for the synthesis of Example 23, replacing ((2-chloroethyl)sulfonyl)benzene with the appropriate alkyl halide. Reactions were conducted at 70° C., and monitored for completion by LCMS, adjusting reaction durations accordingly. The title compounds were cleanly isolated following C18 reverse phase chromatography using an appropriate gradient.

TABLE B MS (apci) Ex # Structure Chemical Name m/z 24

4-(6-(4-(2- isopropoxyethyl)piperazin- 1-yl)pyridin-3-yl)-6-(1- methyl-1H-pyrazol-4- yl)pyrazolo[1,5-a]pyrazine- 3-carbonitrile 472.2 (M + H) 25

4-(6-(4-((6-methoxypyridin- 2-yl)methyl)piperazin-1- yl)pyridin-3-yl)-6-(1- methyl-1H-pyrazol-4- yl)pyrazolo[1,5-a]pyrazine- 3-carbonitrile 507.2 (M + H) 26

4-(6-(4-((2-methoxypyridin- 4-yl)methyl)piperazin-1- yl)pyridin-3-yl)-6-(1- methyl-1H-pyrazol-4- yl)pyrazolo[1,5-a]pyrazine- 3-carbonitrile 507.2 (M + H)

Example 27

4-(6-(4-Benzylpiperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

A suspension of 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile dihydrochloride (Example 8; 20 mg, 0.044 mmol) in anhydrous DMF (0.1 mL) was treated with TEA (18.2 μL, 0.131 mmol) and (bromomethyl)benzene (6.74 μL, 0.0567 mmol). The mixture was stirred 1 h at RT, then purified directly by C18 reverse phase chromatography (using 0-80% ACN/water as the gradient eluent) to afford the title compound (10 mg, 48% yield). MS (apci) m/z=476.2 (M+H).

Example 28

4-(6-(4-(2-((4-Fluorophenyl)sulfonyl)ethyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

A suspension of 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile dihydrochloride (Example 8; 19 mg, 0.042 mmol) in anhydrous DMA (0.5 mL) was treated with TEA (57.8 μL, 0.415 mmol) and 1-((2-chloroethyl)sulfonyl)-4-fluorobenzene (27.7 mg, 0.124 mmol). The mixture was stirred at 70° C. until LCMS indicated complete consumption of carbonitrile. After cooling to ambient temperature, the reaction mixture was quenched by partitioning between water and CHCl₃. The quenched mixture was extracted with CHCl₃ (3×) in a PS Frit, and the combined organic extracts were concentrated in vacuo. The residue was purified by C18 reverse phase chromatography (using 15-80% ACN/water as the gradient eluent) to cleanly afford the title compound (18.7 mg, 79% yield). MS (apci) m/z=572.2 (M+H).

Example 29

4-(6-(4-(3-Methoxybenzyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

A cold (0° C.) suspension of 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile dihydrochloride (Example 8; 15.3 mg, 0.0334 mmol) in anhydrous DMA (0.4 mL) was treated with TEA (18.6 μL, 0.134 mmol) and stirred for 4 min at 0° C. 1-(Bromomethyl)-3-methoxybenzene (0.007011 ml, 0.05007 mmol) was introduced, and the mixture was stirred 3 d at ambient temperature. The reaction mixture was quenched by partitioning between water and CHCl₃. The quenched mixture was extracted with CHCl₃ (3×) in a PS Frit, and the combined organic extracts were concentrated in vacuo. The residue was purified by C18 reverse phase chromatography (using 20-80% ACN/water as the gradient eluent) to cleanly afford the title compound (5.8 mg, 33% yield). MS (apci) m/z=506.2 (M+H).

Example 30

4-(6-(4-(2-Ethoxyethyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

A suspension of 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile dihydrochloride (Example 8; 30 mg, 0.078 mmol) in DMF (778 μL) was treated with K₂CO_(3(s)) (32.3 mg, 0.234 mmol) and 1-bromo-2-ethoxyethane (10.5 μL, 0.0934 mmol). The reaction mixture was stirred overnight at 50° C. After cooling to ambient temperature, the reaction mixture was diluted with MeOH, and filtered. The filtrate was concentrated in vacuo, and the residue was purified by C18 reverse phase chromatography (using 5-95% ACN/water with 0.1% TFA as the gradient eluent) to provide the TFA salt of the title compound. The TFA salt was neutralized by treatment with saturated NaHCO_(3(aq)), and subsequent extraction with EtOAc (3×). The combined organic extracts were dried over anhydrous Na₂SO_(4(s)), filtered, and concentrated in vacuo cleanly afford the title compound (7 mg, 18% yield). MS (apci) m/z=458.2 (M+H).

Example 31

4-(6-(4-Ethylpiperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

A suspension of 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile dihydrochloride (Example 8; 10 mg, 0.0259 mmol in DMF (259 μL) was treated sequentially with K₂CO_(3(s)) (10.8 mg, 0.0778 mmol) and bromoethane (2.31 μL, 0.0311 mmol). The reaction mixture was stirred for 7 d at 50° C. before additional bromoethane (1.93 μL, 0.0259 mmol) was added. After stirring for an additional 4 h at 50° C., the reaction mixture was cooled to ambient temperature and partitioned between DCM (5 mL) and water (5 mL). The mixture was extracted with DCM (3×10 mL). The combined organic extracts were washed with brine, then dried over anhydrous Na₂SO_(4(s)), filtered, and concentrated in vacuo. The residue was purified by silica chromatography (using 5-95% ACN/water with 0.1% TFA as the gradient eluent) to provide the TFA salt of the title compound. The TFA salt was treated with saturated NaHCO_(3(aq)), and subsequently extracted into EtOAc (3×). The combined organic extracts were dried over anhydrous Na₂SO_(4(s)), filtered, and concentrated in vacuo. The residue was purified by silica chromatography (using 0-100% (20% MeOH/2% NH₄OH/78% DCM) in DCM as the gradient eluent) to cleanly afford the title compound (3.9 mg, 36% yield). MS (apci) m/z=414.2 (M+H).

Example 32

4-(6-(4-(2-(tert-butoxy)ethyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-IH-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

A suspension of 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile dihydrochloride (Example 8; 18 mg, 0.039 mmol) in anhydrous DMF (0.4 mL) was treated with 2-(tert-butoxy)ethyl methanesulfonate (23.1 mg, 0.118 mmol) and TEA (54.7 μL, 0.393 mmol). The mixture was stirred for 4 d at 70° C., then cooled to ambient temperature and purified directly by C18 reverse phase chromatography (using 30-85% ACN/water as the gradient eluent) to afford the title compound (3.6 mg, 19% yield). MS (apci) m/z=486.2 (M+H).

Example 33

(R)-4-(6-(4-(2-Hydroxypropyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

A suspension of 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile dihydrochloride (Example 8; 32.5 mg, 0.0709 mmol) in dry MeOH (0.35 mL) was treated sequentially with DIEA (24.8 μL, 0.142 mmol) and (R)-2-methyloxirane (6 μL, 0.0851 mmol). The mixture was stirred for 20 min each first at 75° C., then at ambient temperature. Additional DIEA (24.8 μL, 0.142 mmol), (R)-2-methyloxirane (10 μL, 0.142 mmol) and dry MeOH (0.35 mL) were introduced. The reaction mixture was stirred 3 d at 75° C., then cooled to ambient temperature and concentrated in vacuo. The residue was purified by C18 reverse phase chromatography (using 10-70% ACN/water with 0.1% formic acid as the gradient eluent) to afford the title compound (17 mg, 54% yield). MS (apci) m/z=444.1 (M+H).

Example 34

(S)-4-(6-(4-(2-Hydroxypropyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

The title compound (13 mg, 41% yield) was prepared and purified using a similar procedure to that described for Example 33, replacing (R)-2-methyloxirane with (S)-2-methyloxirane. MS (apci) m/z=501.2 (M+H).

Example 35

4-(6-(4-((6-Methoxypyridin-3-yl)methyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

A suspension of 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile dihydrochloride (Example 8; 115 mg, 0.251 mmol) in dry DMA (2 mL) was treated with TEA (24.8 μL, 0.142 mmol), Me₄N(AcO)₃BH (132 mg, 0.502 mmol) and 6-methoxynicotinaldehyde (72.4 mg, 0.502 mmol). The mixture was stirred for 2 d at ambient temperature before introducing additional TEA (24.8 μL, 0.142 mmol) and Me₄N(AcO)₃BH (132 mg, 0.502 mmol). The reaction mixture was stirred at ambient temperature until starting material had been consumed as determined by LCMS. The reaction mixture was quenched with water/CHCl₃ and extracted with CHCl₃ in a PS Frit. The combined organic extracts were concentrated in vacuo, and the residue was purified by C18 reverse phase chromatography (using 15-80% ACN/water as the gradient eluent) to afford the title compound (6.7 mg, 53% yield). MS (apci) m/z=507.2 (M+H).

The compounds in Table C were prepared using a similar method to that described for the synthesis of Example 35, replacing 6-methoxynicotinaldehyde with the appropriate aldehyde. Reactions were monitored for completion by LCMS, and the timing of the introduction of supplemental reagent amounts, and reaction durations were adjusted accordingly. The title compounds were cleanly isolated following C18 reverse phase chromatography using an appropriate gradient.

TABLE C MS (apci) Ex # Structure Chemical Name m/z 36

6-(1-methyl-1H-pyrazol-4- yl)-4-(6-(4-(pyrimidin-2- ylmethyl)piperazin-1- yl)pyridin-3- yl)pyrazolo[1,5-a]pyrazine- 3-carbonitrile 478.2 (M + H) 37

4-(6-(4-((2- methoxypyrimidin-5- yl)methyl)piperazin-1- yl)pyridin-3-yl)-6-(1- methyl-1H-pyrazol-4- yl)pyrazolo[1,5-a]pyrazine- 3-carbonitrile 508.2 (M + H) 38

4-(6-(4-((6- (dimethylamino)pyridin-3- yl)methyl)piperazin-1- yl)pyridin-3-yl)-6-(1- methyl-1H-pyrazol-4- yl)pyrazolo[1,5-a]pyrazine- 3-carbonitrile 520.3 (M + H)

Example 39

6-(1-Methyl-1H-pyrazol-4-yl)-4-(6-(4-(pyridin-2-ylmethyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

A suspension of 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile dihydrochloride (Example 8; 2.0 g, 4.4 mmol) in dry DMA (44 mL) was treated sequentially with TEA (1.82 mL, 13.1 mmol) and NaBH(AcO)₃ (132 mg, 0.502 mmol). The mixture was treated, in dropwise fashion, with picolinaldehyde (0.935 g, 8.73 mmol), and stirred for 4 h at ambient temperature. The reaction mixture was poured slowly into cold (0° C.) DI water (500 mL), and the quenched mixture was stirred overnight at ambient temperature before vacuum filtering. The resultant filter cake was rinsed with water (100 mL) and MTBE (100 mL). The solids then were dissolved in DCM, dried over anhydrous Na₂SO_(4(s)), filtered, and concentrated in vacuo to cleanly afford the title compound (1.70 g, 82% yield). MS (apci) m/z=477.2 (M+H).

Example 40

6-(1-Methyl-1H-pyrazol-4-yl)-4-(6-(4-((6-methylpyridin-2-yl)methyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

A suspension of 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile dihydrochloride (Example 8; 50 mg, 0.11 mmol) in dry DMA (1.1 mL) was treated sequentially with TEA (1.82 mL, 13.1 mmol), 6-methylpicolinaldehyde (26.4 mg, 0.218 mmol) and NaBH(AcO)₃ (132 mg, 0.502 mmol). The mixture was stirred for 18 h at ambient temperature. The reaction mixture was poured dropwise into rapidly stirring DI water (20 mL), and the quenched mixture was stirred overnight at ambient temperature before vacuum filtering. The resultant filter cake was rinsed with water (3×5 mL) and MTBE (3×5 mL). The solids were dissolved in DCM, dried over anhydrous Na₂SO_(4(s)), filtered, and concentrated in vacuo to cleanly afford the title compound (43.4 mg, 77% yield). MS (apci) m/z=491.3 (M+H).

Example 41

6-(1-Methyl-1H-pyrazol-4-yl)-4-(6-(4-((tetrahydro-2H-pyran-4-yl)methyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile 2,2,2-trifluoroacetate

A suspension of 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile dihydrochloride (Example 8; 50 mg, 0.11 mmol) in DCE (259 μL) was treated sequentially with tetrahydro-2H-pyran-4-carbaldehyde (6 μL, 0.052 mmol) and NaBH(AcO)₃ (132 mg, 0.502 mmol). The mixture was stirred for 5 h at ambient temperature. The reaction mixture was concentrated in vacuo, and the residue was purified by C18 reverse phase chromatography (using 5-95% ACN/water with 0.1% TFA the gradient eluent) to cleanly afford the title compound (2.7 mg, 22% yield). MS (apci) m/z=484.2 (M+H).

Example 42

4-(6-(4-((1-Methyl-1H-benzo[d]imidazol-5-yl)methyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

A suspension of 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile dihydrochloride (Example 8; 30 mg, 0.078 mmol) in DCE (778 μL) was treated sequentially with 1-methyl-1H-benzimidazole-5-carboxaldehyde (25 mg, 0.16 mmol) and NaBH(AcO)₃ (49 mg, 0.23 mmol). The mixture was stirred overnight at ambient temperature, and then concentrated in vacuo. The residue was purified first by silica chromatography (using 0-20% MeOH in DCM as the gradient eluent) and then by C18 reverse phase chromatography (using 5-95% ACN/water with 0.1% TFA the gradient eluent) to cleanly afford the title compound as its TFA salt. The TFA salt was treated with saturated NaHCO_(3(aq)), and subsequently extracted into EtOAc (3×). The combined organic extracts were dried over anhydrous Na₂SO_(4(s)), filtered, and concentrated in vacuo to cleanly afford the title compound (1.5 mg, 3.6% yield). MS (apci) m/z=529.8 (M+H).

Example 43

(S)-4-(6-(3-Hydroxypiperidin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

A solution of 4-(6-fluoropyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile (Intermediate P7; 50 mg, 0.16 mmol) in DMSO (3.1 mL) was treated with (S)-piperidin-3-ol (79 mg, 0.78 mmol) and K₂CO_(3(s)) (87 mg, 0.63 mmol) then stirred overnight at 110° C. After cooling to ambient temperature, the reaction mixture was diluted with water (10 mL), and extracted with DCM (4×10 mL) in a PS Frit. The combined organic extracts were concentrated in vacuo, and purified by C18 reverse phase chromatography (using 0-60% ACN/water as the gradient eluent) to afford the title compound (35 mg, 56% yield). MS (apci) m/z=401.1 (M+H).

Example 44

tert-Butyl (S)-(1-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperidin-3-yl)(methyl)carbamate

A solution of 4-(6-fluoropyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile (Intermediate P7; 0.100 g, 0.313 mmol) in DMSO (6.26 mL) was treated with (S)-tert-butyl methyl(piperidin-3-yl)carbamate (0.268 g, 1.25 mmol) and K₂CO_(3(s)) (0.173 g, 1.25 mmol) and stirred overnight at 110° C. After cooling to ambient temperature, the reaction mixture was diluted with water (10 mL) and extracted with DCM (4×10 mL) in a PS Frit. The combined organic extracts were concentrated in vacuo, and purified by C18 reverse phase chromatography (using 0-60% ACN/water as the gradient eluent) to afford the title compound (106 mg, 66% yield). MS (apci) m/z=514.2 (M+H).

Example 45

(S)-6-(1-Methyl-1H-pyrazol-4-yl)-4-(6-(3-(methylamino)piperidin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile dihydrochloride

A solution of tert-butyl (S)-(1-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperidin-3-yl)(methyl)carbamate (Example 44; 100 mg, 0.195 mmol) in CHCl₃ (2 mL) was treated 5 M HCl in iPrOH (195 μL, 0.974 mmol). The mixture was stirred 2 h at ambient temperature, and then concentrated in vacuo to afford the title compound (80 mg, 99% yield). MS (apci) m/z=414.2 (M+H).

Example 46

6-(1-Methyl-1H-pyrazol-4-yl)-4-(6-((3S,4S)-4-methyl-3-(methylamino)piperidin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile dihydrochloride

Step 1: Preparation of tert-Butyl ((3S,4S)-1-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)-4-methylpiperidin-3-yl)(methyl)carbamate. A solution of 4-(6-fluoropyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile (Intermediate P7; 0.100 g, 0.313 mmol) in DMSO (6.26 mL) was treated with tert-butyl methyl((3S,4S)-4-methylpiperidin-3-yl)carbamate (0.100 g, 0.438 mmol) and K₂CO_(3(s)) (0.173 g, 1.25 mmol) and stirred overnight at 110° C. After cooling to ambient temperature, the reaction mixture was diluted with water (10 mL) and extracted with DCM (4×10 mL) in a PS Frit. The combined organic extracts were concentrated in vacuo and purified by C18 reverse phase chromatography (using 0-80% ACN/water as the gradient eluent) to afford the title compound (32 mg, 19% yield). MS (apci) m/z=528.3 (M+H).

Step 2: Preparation of 6-(1-Methyl-1H-pyrazol-4-yl)-4-(6-((3S,4S)-4-methyl-3-(methylamino)piperidin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile dihydrochloride. A solution of tert-butyl ((3S,4S)-1-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)-4-methylpiperidin-3-yl)(methyl)carbamate (Example 46. Step 1; 10 mg, 0.020 mmol) in CHCl₃ (2 mL) was treated 5 M HCl in iPrOH (11 μL, 0.057 mmol). The mixture was stirred overnight at ambient temperature, and then concentrated in vacuo. The residue was washed with Et₂O (2×1 mL) and air-dried to afford the title compound (6 mg, 74% yield). MS (apci) m/z=414.2 (M+H).

Example 47

4-(6-(4-((6-Methoxypyridin-3-yl)methyl)piperazin-1-yl)pyridin-3-yl)-6-(1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile 2,2,2-trifluoroacetate

Step 1: Preparation of 6-(1-(4-Methoxybenzyl)-1H-pyrazol-4-yl)-4-(6-(4-((6-methoxypyridin-3-yl)methyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile. A mixture of 4-chloro-6-(1-(4-methoxybenzyl)-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile (Intermediate P4; 270 mg, 0.740 mmol), 1-((6-methoxypyridin-3-yl)methyl)-4-(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)piperazine (456 mg, 1.11 mmol), Na₂CO_(3(s)) (0.392 g, 3.70 mmol) and Pd(PPh₃)₄ (0.0428 g, 0.0370 mmol) was suspended in 1,4-dioxane (9.72 mL) and sparged with Ar_((g)). The mixture was stirred 2 h at 80° C. before water (0.5 mL) and additional Pd(PPh₃)₄ were introduced. The reaction mixture was sparged again with Ar_((g)) and stirred for 2 d at 80° C. The reaction mixture was cooled to ambient temperature, then diluted with DCM and washed with water. The organic extracts were purified by silica chromatography (10% to 100% EtOAc in DCM) to cleanly afford the title compound (291 mg, 64% yield). MS (apci) m/z=612.8 (M+H).

Step 2: Preparation of 4-(6-(4-((6-Methoxypyridin-3-yl)methyl)piperazin-1-yl)pyridin-3-yl)-6-(1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile 2,2,2-trifluoroacetate. Under N_(2(g)), 6-(1-(4-methoxybenzyl)-1H-pyrazol-4-yl)-4-(6-(4-((6-methoxypyridin-3-yl)methyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile (291 mg, 0.475 mmol) was suspended in TFA (20 mL) then stirred overnight at 90° C. After cooling to ambient temperature, the reaction mixture was azeotroped with toluene (2×5 mL) in vacuo. The residue was purified by C18 reverse phase chromatography (using 2-50% ACN/water with 0.1% TFA as the gradient eluent) and dried under high vacuum overnight to afford the title compound (296 mg, quantitative yield). MS (apci) m/z=493.2 (M+H).

Example 48

6-(1-(Azetidin-3-yl)-1H-pyrazol-4-yl)-4-(6-(4-((6-methoxypyridin-3-yl)methyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile 2,2,2-trifluoroacetate

A solution of 4-(6-(4-((6-methoxypyridin-3-yl)methyl)piperazin-1-yl)pyridin-3-yl)-6-(1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile 2,2,2-trifluoroacetate (Example 47; 29 mg, 0.059 mmol) in DMA (1 mL) was treated sequentially with Cs₂CO_(3(s)) (58 mg, 0.18 mmol) and tert-butyl 3-iodoazetidine-1-carboxylate (20.0 mg, 0.0707 mmol). The mixture was stirred 1.5 h at 80° C. before introducing additional tert-butyl 3-iodoazetidine-1-carboxylate (6.7 mg, 0.071 mmol). The reaction was stirred for 3 d at 80° C., then concentrated in vacuo and suspended 1:1 DCM:water (2 mL). The organic extracts were separated, then washed with water (2×1 mL), dried over anhydrous MgSO_(4(s)), filtered, and concentrated in vacuo. The residue was dissolved in 1:1 TFA:DCM (2 mL), stirred 30 min at ambient temperature, and concentrated in vacuo to cleanly afford the title compound (37.2 mg, 96% yield). MS (apci) m/z=548.2 (M+H).

Example 49

4-(6-(4-((6-Methoxypyridin-3-yl)methyl) piperazin-1-yl)pyridin-3-yl)-6-(1-(1-methylazetidin-3-yl)-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

A solution of 6-(1-(azetidin-3-yl)-1H-pyrazol-4-yl)-4-(6-(4-((6-methoxypyridin-3-yl)methyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile 2,2,2-trifluoroacetate 2,2,2-trifluoroacetate (Example 48; 28 mg, 0.042 mmol) in MeOH (1.0 mL) and formaldehyde (6.9 μL, 0.093 mmol) was stirred for 30 min at ambient temperature, then treated with NaBH(AcO)₃ (27 mg, 0.13 mmol). The mixture was stirred for 3 h at ambient temperature before introducing additional NaBH(AcO)₃ (28 mg, 0.13 mmol) and formaldehyde (6.9 μL, 0.093 mmol). The reaction was stirred for 18 h at ambient temperature, then concentrated in vacuo and suspended 1:1 DCM:water (2 mL). The organic extracts were separated, then washed with water (2×1 mL), dried over anhydrous MgSO_(4(s)), filtered, and concentrated in vacuo to cleanly afford the title compound (4.8 mg, 20% yield). MS (apci) m/z=562.3 (M+H).

Example 50

6-(1-(2-(Isopropylsulfonyl)ethyl)-1H-pyrazol-4-yl)-4-(6-(4-((6-methoxypyridin-3-yl)methyl) piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

A solution of 4-(6-(4-((6-methoxypyridin-3-yl)methyl)piperazin-1-yl)pyridin-3-yl)-6-(1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile 2,2,2-trifluoroacetate (Example 47; 29 mg, 0.059 mmol) in DMA (1 mL) was treated sequentially with Cs₂CO_(3(s)) (58 mg, 0.18 mmol) and 2-((2-chloroethyl)sulfonyl)propane (12.1 mg, 0.0707 mmol). The mixture was stirred for 1 h at 80° C., then concentrated in vacuo and suspended 1:1 DCM:water (2 mL). The organic extracts were separated, then washed with water (2×1 mL), dried over anhydrous MgSO_(4(s)), filtered, concentrated in vacuo to cleanly afford the title compound (16.4 mg, 44% yield). MS (apci) m/z=627.2 (M+H).

The compounds in Table D were prepared using a similar method to that described for the synthesis of Example 50, replacing 2-((2-chloroethyl)sulfonyl)propane with the appropriate alkyl halide (except where noted *). Reactions were monitored for completion by LCMS, and reaction durations were adjusted accordingly.

TABLE D MS (apci) Ex # Structure Chemical Name m/z 51

4-(6-(4-((6-methoxypyridin- 3-yl)methyl)piperazin-1- yl)pyridin-3-yl)-6-(1- ((tetrahydro-2H-pyran-4- yl)methyl)-1H-pyrazol-4- yl)pyrazolo[1,5-a]pyrazine- 3-carbonitrile 591.3 (M + H) 52

4-(6-(4-((6-methoxypyridin- 3-yl)methyl)piperazin-1- yl)pyridin-3-yl)-6-(1-(2- morpholinoethyl)-1H- pyrazol-4-yl)pyrazolo[1,5- a]pyrazine-3-carbonitrile 606.3 (M + H) 53

6-(1-(2-isopropoxyethyl)- 1H-pyrazol-4-yl)-4-(6-(4- ((6-methoxypyridin-3- yl)methyl)piperazin-1- yl)pyridin-3- yl)pyrazolo[1,5-a]pyrazine- 3-carbonitrile 579.3 (M + H) * after 1.5 h reaction, required the introduction of supplemental alkylating agent (1.2 equivalents) and additional stirring (3 d) at ambient temperature to achieve completion

Example 54

6-(1-(2-Methoxyethyl)-1H-pyrazol-4-yl)-4-(6-(4-((6-methoxypyridin-3-yl)methyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

A solution of 4-(6-(4-((6-methoxypyridin-3-yl)methyl)piperazin-1-yl)pyridin-3-yl)-6-(1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile 2,2,2-trifluoroacetate (Example 47; 29 mg, 0.059 mmol) in DMA (1 mL) was treated sequentially with Cs₂CO_(3(s)) (58 mg, 0.18 mmol) and 1-chloro-2-methoxyethane (6.7 mg, 0.071 mmol). The mixture was stirred 1.5 h at 80° C. before introducing additional 1-chloro-2-methoxyethane (6.7 mg, 0.071 mmol). The reaction was stirred 3 d at 80° C., then directly purified by preparative thin layer silica chromatography (using 1:1:8 MeOH/Acetone/DCM as eluent) to cleanly afford the title compound (7.7 mg, 24% yield). MS (apci) m/z=551.3 (M+H).

The compounds in Table E were prepared using a similar method to that described for the synthesis of Example 54, replacing 1-chloro-2-methoxyethane with the appropriate alkyl halide. Reactions were monitored for completion by LCMS, and reaction durations were adjusted accordingly. Title compounds were cleanly isolated following preparative thin layer silica chromatography using an appropriate eluent.

TABLE E MS (apci) Ex # Structure Chemical Name m/z 55

4-(6-(4-((6- methoxypyridin-3- yl)methyl)piperazin- 1-yl)pyridin-3-yl)-6- (1-((tetrahydro-2H- pyran-2-yl)methyl)- 1H-pyrazol-4- yl)pyrazolo[1,5- a]pyrazine-3- carbonitrile 591.3 (M + H) 56

4-(6-(4-((6- methoxypyridin-3- yl)methyl)piperazin- 1-yl)pyridin-3-yl)-6- (1-(tetrahydro-2H- pyran-4-yl)-1H- pyrazol-4- yl)pyrazolo[1,5- a]pyrazine-3- carbonitrile 577.3 (M + H) 57

4-(6-(4-((6- methoxypyridin-3- yl)methyl)piperazin- 1-yl)pyridin-3-yl)-6- (1-(oxetan-3-yl)-1H- pyrazol-4- yl)pyrazolo[1,5- a]pyrazine-3- carbonitrile 549.3 (M + H)

Example 58

4-((1-(5-(6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperidin-4-yl)oxy)benzonitrile

A solution of 4-(6-fluoropyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine (Intermediate P5; 14.2 mg, 0.0482 mmol) in DMA (0.1 mL) was treated with TEA (6.72 μL, 0.0482 mmol) and 4-(piperidin-4-yloxy)benzonitrile (20 mg, 0.0989 mmol) then stirred overnight at 110° C. After cooling to ambient temperature, the reaction mixture was diluted with water (10 mL), and extracted with DCM (4×10 mL) in a PS Frit. The combined organic extracts were concentrated in vacuo, and purified by C18 reverse phase chromatography (using 0-60% ACN/water as the gradient eluent) to afford the title compound (3.0 mg, 13.1% yield). MS (apci) m/z=477.2 (M+H).

Example 59

6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(4-(pyridin-2-yloxy)piperidin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine

A solution of 4-(6-fluoropyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine (Intermediate P5; 31.5 mg, 0.107 mmol) in DMA (0.1 mL) was treated with TEA (74.5 μL, 0.534 mmol) and 2-(piperidin-4-yloxy)pyridine (20 mg, 0.112 mmol), then stirred overnight at 110° C. After cooling to ambient temperature, the reaction mixture was diluted with water (10 mL), and extracted with DCM (4×10 mL) in a PS Frit. The combined organic extracts were concentrated in vacuo, and purified by C18 reverse phase chromatography (using 0-60% ACN/water as the gradient eluent) to afford the title compound (8.4 mg, 17% yield). MS (apci) m/z=453.3 (M+H).

Example 60

4-(6-(4-(2-amino-2-(3-chlorophenyl)acetyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

Step 1: Preparation of tert-butyl (1-(3-chlorophenyl)-2-(4-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperazin-1-yl)-2-oxoethyl)carbamate. A mixture of 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile (Example 8; 400 mg, 0.802 mmol), N-Boc-(3′-chlorophenyl)glycine (229 mg, 0.802 mmol) and HATU (915 mg, 2.41 mmol) in anhydrous DCM (0.4 mL) was treated sequentially with DIEA (140 μL, 0.802 mmol) and anhydrous DMF (250 μL). The resulting mixture was stirred for 1 h at ambient temperature and then concentrated in vacuo. The crude material was purified by reverse phase chromatography (5-95% ACN in water with 0.1% TFA), and fractions containing the desired product were combined and extracted with 4:1 DCM:iPrOH. The organic extracts were concentrated in vacuo to afford the title compound in sufficient purity for subsequent use (524 mg, quantitative yield). MS (apci) m/z=653.3 (M+H).

Step 2: Preparation of 4-(6-(4-(2-amino-2-(3-chlorophenyl)acetyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile. A solution of tert-butyl (1-(3-chlorophenyl)-2-(4-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperazin-1-yl)-2-oxoethyl)carbamate (Step 1; 1.0 g, 1.5 mmol) in DCM (15 mL) was treated with TFA (1.2 mL, 15 mmol). The reaction mixture was stirred for a period of 5 h at ambient temperature, introducing additional TFA (5 equivalents) at the 1 h and 4 h time intervals. The resulting mixture then was stirred overnight at ambient temperature, and concentrated in vacuo. The residue was purified by C18 reverse phase chromatography (using 5-95% water: ACN as the gradient eluent). Fractions containing the desired product were combined, diluted with 4:1 DCM: iPrOH, and sequentially washed with saturated NaHCO_(3(aq)) and brine. The combined organic extracts were dried over anhydrous Na₂SO_(4(s)), filtered, and concentrated in vacuo to afford the semi-pure title compound. The semi-pure material was triturated with DCM/Hexanes (1:10) to afford the title compound (435 mg, 51% yield). MS (apci) m/z=554.2 (M+H).

Example 61

4-(6-(4-(2-amino-2-(4-chlorophenyl)acetyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

Step 1: Preparation of tert-butyl (1-(4-chlorophenyl)-2-(4-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperazin-1-yl)-2-oxoethyl)carbamate. A suspension of 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile 2,2,2-trifluoroacetate (Example 8; 60 mg, 0.12 mmol), (S)-2-((tert-butoxycarbonyl)amino)-2-(4-chlorophenyl)acetic acid (34 mg, 0.12 mmol) and HATU (137 mg, 0.36 mmol) in anhydrous DCM (0.6 mL) was treated with 4-methylmorpholine (40 μL, 0.36 mmol). The reaction mixture was stirred overnight at ambient temperature, and then filtered. The resultant filtrate was subjected to C18 reverse phase chromatography (using 5-95% water:ACN as the gradient eluent to cleanly afford the title compound (72 mg, 92% yield). MS (apci) m/z=653.3 (M+H).

Step 2: Preparation of 4-(6-(4-(2-amino-2-(4-chlorophenyl)acetyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile. A solution of tert-butyl (1-(4-chlorophenyl)-2-(4-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperazin-1-yl)-2-oxoethyl)carbamate (Step 1; 72 mg, 0.11 mmol) in DCM (1.1 mL) was treated with TFA (85 μL, 1.1 mmol). The resulting mixture was stirred for 3 h at ambient temperature, and subsequently concentrated in vacuo. The residue was purified by C18 reverse phase chromatography (using 5-95% water: ACN as the gradient eluent). Fractions containing the desired product were combined, diluted with 4:1 DCM: iPrOH, and sequentially washed with saturated NaHCO_(3(aq)) and brine. The combined organic extracts were dried over anhydrous Na₂SO_(4(s)), filtered, and concentrated in vacuo to afford semi-pure title compound. The semi-pure material was triturated with DCM/Hexanes (1:10) to afford the title compound (37 mg, 61% yield). MS (apci) m/z=553.2 (M+H).

Example 62

(R)-4-(6-(4-(2-amino-2-(4-fluorophenyl)acetyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

Step 1: Preparation of tert-butyl (R)-(2-(4-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperazin-1-yl)-1-(4-fluorophenyl)-2-oxoethyl)carbamate. A mixture of 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile dihydrochloride (Example 8; 50 mg, 0.11 mmol), (R)-2-((tert-butoxycarbonyl)amino)-2-(4-fluorophenyl)acetic acid (29 mg, 0.11 mmol) and HATU (50 mg, 0.13 mmol) in anhydrous DCM (7.0 μL) was treated with DIEA (19 μL, 0.11 mmol). The reaction mixture was stirred overnight at ambient temperature, and then was concentrated in vacuo. The residue was purified by silica chromatography (using 0-10% CHCl₃/MeOH with 0.1% NH₄OH as the gradient eluent) to afford the title compound which was used directly in Step 2 (75 mg, quantitative yield). MS (apci) m/z=537.2 (M+H).

Step 2: Preparation of (R)-4-(6-(4-(2-amino-2-(4-fluorophenyl)acetyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile. A solution of tert-butyl (R)-(2-(4-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperazin-1-yl)-1-(4-fluorophenyl)-2-oxoethyl)carbamate (Step 1; 75 mg, 0.12 mmol) in DCM (236 μL) was treated with TFA (91 μL, 1.2 mmol). The resulting mixture was stirred 30 min at ambient temperature before introducing additional TFA (10 equivalents). The reaction mixture was stirred for 1 h at ambient temperature, and then concentrated in vacuo. The residue was purified by silica chromatography (using 0-10% CHCl₃/MeOH with 0.1% NH₄OH as the gradient eluent) to afford the title compound (37 mg, 59% yield). MS (apci) m/z=537.2 (M+H).

Example 63

4-(6-(4-(2-amino-2-(2-fluorophenyl)acetyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

Step 1: Preparation of tert-butyl (2-(4-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-V)pyrazolo[1,5-a]pyrazin-4-v)pyridin-2-yl)piperazin-1-yl)-1-(2-fluorophenyl)-2-oxoethyl)carbamate. A mixture of 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile (Example 8; 100 mg, 0.259 mmol), 2-((tert-butoxycarbonyl)amino)-2-(2-fluorophenyl)acetic acid (Intermediate R2; 69.9 mg, 0.259 mmol) and HATU (296 mg, 0.778 mmol) in anhydrous DCM (1.3 mL) was treated with DIEA (181 μL, 1.04 mmol). The resulting mixture was stirred for 1 h at ambient temperature. The resulting suspension was filtered, and the filtrate was purified by C18 reverse phase chromatography (using 5-95% water: ACN with 0.1% TFA as the gradient eluent). Fractions containing the desired product were combined, diluted with 4:1 DCM:iPrOH and washed with brine. The organic extracts were dried over anhydrous Na₂SO_(4(s)), filtered, and concentrated in vacuo to afford the title compound in sufficient purity for subsequent use (165 mg, quantitative yield). MS (apci) m/z=637.3 (M+H).

Step 2: Preparation of 4-(6-(4-(2-amino-2-(2-fluorophenyl)acetyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile. tert-Butyl (2-(4-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperazin-1-yl)-1-(2-fluorophenyl)-2-oxoethyl)carbamate (Step 1; 165 mg, 0.259 mmol) was dissolved in 1:1 TFA:DCM (2.6 mL). The resulting mixture was stirred overnight at ambient temperature and subsequently concentrated in vacuo. The residue was purified by C18 reverse phase chromatography (using 5-95% water: ACN with 0.1% TFA as the gradient eluent). Fractions containing the desired product were combined, diluted with 4:1 DCM: iPrOH, and sequentially washed with saturated NaHCO_(3(aq)) and brine. The combined organic extracts were dried over anhydrous Na₂SO_(4(s)), filtered, and concentrated in vacuo to afford semi-pure title compound. The semi-pure material was triturated with DCM/Hexanes (1:10) to afford the title compound (46.5 mg, 33.4% yield). MS (apci) m/z=537.2 (M+H).

Example 64

4-(6-(4-(2-amino-2-(2,4-difluorophenyl)acetyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

Step 1: Preparation of tert-butyl (2-(4-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperazin-1-yl)-1-(2,4-difluorophenyl)-2-oxoethyl)carbamate. A mixture of 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile (Example 8; 100 mg, 0.259 mmol), 2-((tert-butoxycarbonyl)amino)-2-(2,4-difluorophenyl)acetic acid (Intermediate R3; 74.5 mg, 0.259 mmol) and HATU (296 mg, 0.778 mmol) in anhydrous DCM (1.3 mL) was treated with DIEA (181 μL, 1.04 mmol). The resulting mixture was stirred for 1 h at ambient temperature, then concentrated in vacuo to afford the title compound in sufficient purity for subsequent use (170 mg, quantitative yield). MS (apci) m/z=655.3 (M+H).

Step 2: Preparation of 4-(6-(4-(2-amino-2-(2,4-difluorophenyl)acetyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile. Crude tert-butyl (2-(4-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperazin-1-yl)-1-(2,4-difluorophenyl)-2-oxoethyl)carbamate (Step 1; 170 mg, 0.260 mmol) was dissolved in 1:1 TFA:DCM (2.6 mL). The resulting mixture was stirred overnight at ambient temperature and subsequently concentrated in vacuo. The residue was purified by C18 reverse phase chromatography (using 5-95% ACN in water with 0.1% TFA as the gradient eluent). Fractions containing the desired product were combined, diluted with 4:1 DCM: iPrOH, and sequentially washed with saturated NaHCO_(3(aq)) and brine. The combined organic extracts were dried over anhydrous Na₂SO_(4(s)), filtered, and concentrated in vacuo to afford semi-pure title compound. The semi-pure material was triturated with DCM/Hexanes (1:10) to afford the title compound (89 mg, 62% yield). MS (apci) m/z=555.2 (M+H).

Example 65

4-(6-(4-(2-amino-2-(3-chloro-4-fluorophenyl)acetyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

Step 1: Preparation of tert-butyl (1-(3-chloro-4-fluorophenyl)-2-(4-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperazin-1-yl)-2-oxoethyl)carbamate. A mixture of 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile dihydrochloride (Example 8; 200 mg, 0.436 mmol), 2-((tert-butoxycarbonyl)amino)-2-(3-chloro-4-fluorophenyl)acetic acid (Intermediate R4; 133 mg, 0.436 mmol) and HATU (498 mg, 1.31 mmol) in anhydrous DCM (2.2 mL) was treated with DIEA (76.2 μL, 0.436 mmol). The reaction mixture was stirred overnight at ambient temperature. The resulting suspension was filtered, and the filtrate was concentrated in vacuo to provide the desired compound (293 mg, quantitative yield). MS (apci) m/z=571.2 (M+H).

Step 2: Preparation of 4-(6-(4-(2-amino-2-(3-chloro-4-fluorophenyl)acetyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile. A solution of tert-butyl (1-(3-chloro-4-fluorophenyl)-2-(4-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperazin-1-yl)-2-oxoethyl)carbamate (Step 1; 293 mg, 0.437 mmol) in DCM (4.4 mL) was treated with TFA (336 μL, 4.37 mmol). The resulting mixture was stirred for 1 h at ambient temperature, and then before additional TFA (10 equivalents) was added. The reaction mixture was stirred for an additional 2 h at ambient temperature, introducing additional TFA (2 mL) after the first additional 1 h of stirring at ambient temperature. The reaction mixture was concentrated in vacuo. The residue was purified by C18 reverse phase chromatography (using 5-95% water: ACN with 0.1% TFA as the gradient eluent). The solid isolated was re-purified by silica chromatography (using 0-10% DCM/MeOH with 0.1% NH₄OH as the gradient eluent) and Fractions containing the desired product were combined and concentrated in vacuo. The residue was triturated with DCM/MeOH (1:10) and the solvents were removed in vacuo to afford the title compound (152 mg, 61% yield). MS (apci) m/z=571.2 (M+H).

Example 66

(R)-4-(6-(4-(2-amino-2-phenylpropanoyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

Step 1: Preparation of tert-butyl (R)-(1-(4-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperazin-1-yl)-1-oxo-2-phenylpropan-2-yl)carbamate. A mixture of 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile (Example 8; 60 mg, 0.16 mmol), (R)-2-((tert-butoxycarbonyl)amino)-2-phenylpropanoic acid (41 mg, 0.16 mmol) and HATU (71 mg, 0.19 mmol) in anhydrous DCM (1.6 mL) was treated with DIEA (82 μL, 0.47 mmol). The reaction mixture was stirred overnight at ambient temperature. The resulting suspension was concentrated in vacuo to afford the title compound in sufficient purity for subsequent use (98 mg, 99% yield). MS (apci) m/z=633.3 (M+H).

Step 2: Preparation of (R)-4-(6-(4-(2-amino-2-phenylpropanoyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile. A solution of tert-butyl (R)-(1-(4-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperazin-1-yl)-1-oxo-2-phenylpropan-2-yl)carbamate (Step 1; 98 mg, 0.15 mmol) in 1:1 TFA:DCM (155 μL) was stirred overnight at ambient temperature, and then concentrated in vacuo. The residue was purified by C18 reverse phase chromatography (using 5-95% water: ACN with 0.1% TFA as the gradient eluent). Fractions containing the desired product were combined, diluted with 4:1 DCM:iPrOH, and sequentially washed with saturated NaHCO_(3(aq)) and brine. The combined organic extracts were dried over anhydrous Na₂SO_(4(s)), filtered, and concentrated in vacuo to afford semi-pure title compound (79 mg, 96% yield) which was carried on without further purification. MS (apci) m/z=533.2 (M+H).

Example 67

(R)-4-(6-(4-(3-amino-2-phenylpropanoyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

Step 1: Preparation of tert-butyl (R)-(3-(4-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperazin-1-yl)-3-oxo-2-phenylpropyl)carbamate. A suspension of 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile (Example 8; 40 mg, 0.10 mmol), (R)-3-(Boc-amino)-2-phenylpropionic acid (28 mg, 0.10 mmol) and HATU (118 mg, 0.31 mmol) in anhydrous DCM (519 μL) was treated with DIEA (73 μL, 0.42 mmol). The reaction mixture was stirred overnight at ambient temperature. The resulting suspension was filtered, and the filtrate was concentrated in vacuo. The residue was purified by silica chromatography (using 0-10% DCM/MeOH with 0.1% NH₄OH as the gradient eluent) to afford the title compound in sufficient purity for subsequent use (78 mg, quantitative yield). MS (apci) m/z=633.3 (M+H).

Step 2: Preparation of (R)-4-(6-(4-(3-amino-2-phenylpropanoyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile. A solution of tert-butyl (R)-(3-(4-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperazin-1-yl)-3-oxo-2-phenylpropyl)carbamate (Step 1; 78 mg, 0.12 mmol) in DCM (7.0 mL) was treated with TFA (95 μL, 1.2 mmol) and stirred overnight at ambient temperature. The resulting suspension was concentrated in vacuo, and the residue was purified by silica chromatography (using 0-10% DCM/MeOH as the gradient eluent). Fractions containing the desired product were combined, concentrated in vacuo and triturated with DCM/Hexanes to cleanly afford the title compound (54 mg, 82% yield). MS (apci) m/z=533.3 (M+H).

Example 68

4-(6-(4-(3-amino-2-(4-fluorophenyl)propanoyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

Step 1: Preparation of tert-butyl (3-(4-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperazin-1-yl)-2-(4-fluorophenyl)-3-oxopropyl)carbamate. A mixture of 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile (Example 8; 100 mg, 0.259 mmol), 3-{[(tert-butoxy)carbonyl]amino}-2-(4-fluorophenyl)propanoic acid (73.5 mg, 0.259 mmol) and HATU (296 mg, 0.778 mmol) in anhydrous DCM (1.3 mL) was treated with DIEA (181 μL, 1.04 mmol). The reaction mixture was stirred for 1 h at ambient temperature. The resulting suspension was filtered, and the filtrate was concentrated in vacuo to afford the title compound in sufficient purity for subsequent use (169 mg, quantitative yield). MS (apci) m/z=651.3 (M+H).

Step 2: Preparation of 4-(6-(4-(3-amino-2-(4-fluorophenyl)propanoyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile. A solution of tert-butyl (3-(4-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperazin-1-yl)-2-(4-fluorophenyl)-3-oxopropyl)carbamate (Step 1; 169 mg, 0.260 mmol) in DCM (2.6 mL) was treated with TFA (0.2 mL, 2.60 mmol). The resulting mixture was stirred for 1 h at ambient temperature and then concentrated in vacuo. The residue was purified by C18 reverse phase chromatography (using 5-95% water: ACN with 0.1% TFA as the gradient eluent). Fractions containing the desired product were combined, diluted with 4:1 DCM: iPrOH, and sequentially washed with saturated NaHCO_(3(aq)) and brine. The combined organic extracts were dried over anhydrous Na₂SO_(4(s)), filtered, and concentrated in vacuo to afford semi-pure title compound. The semi-pure material was triturated with DCM/Hexanes (1:10) to afford the title compound (143 mg, quantitative yield). MS (apci) m/z=551.3 (M+H).

Example 69

6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(4-((2S)-2-phenyl-2-(pyrrolidin-2-yl)acetyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

Step 1: Preparation of tert-butyl 2-((S)-2-(4-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-ylpyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperazin-1-yl)-2-oxo-1-phenylethyl)pyrrolidine-1-carboxylate. A suspension of 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile (Example 8; 275.0 mg, 0.7135 mmol) in anhydrous DCM (7.0 mL) was treated with (2S)-2-(1-(tert-butoxycarbonyl)pyrrolidin-2-yl)-2-phenylacetic acid (Intermediate R5; 239.7 mg, 0.7848 mmol), HATU (298.4 mg, 0.7848 mmol) and DIEA (497 μL, 2.85 mmol). The reaction mixture was stirred 16 h at ambient temperature. The resulting solution was concentrated in vacuo, and the residue was purified by silica chromatography (using 5-95% DCM:Acetone as the gradient eluent) to afford the title compound which was used directly in Step 2. MS (apci) m/z=573.3 (M+H).

Step 2: Preparation of 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(4-((2S)-2-phenyl-2-(pyrrolidin-2-yl)acetyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile. A solution of tert-butyl 2-((S)-2-(4-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperazin-1-yl)-2-oxo-1-phenylethyl)pyrrolidine-1-carboxylate (Step 1; 0.713 mmol) in 1:1 TFA:DCM (7.0 mL) was stirred 30 min at ambient temperature, and subsequently concentrated in vacuo. The residue was purified by C18 reverse phase chromatography (using 5-95% water: ACN with 0.1% TFA as the gradient eluent). Fractions containing the desired product were combined, diluted with 4:1 DCM:iPrOH, and sequentially washed with saturated NaHCO_(3(aq)) and brine. The combined organic extracts were dried over anhydrous Na₂SO_(4(s)), filtered, and concentrated in vacuo to cleanly afford the title compound as about 97% of a single enantiomer (250.0 mg, 61% yield). MS (apci) m/z=573.3 (M+H).

Example 70

(R)-6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(4-(2-methylpyrrolidine-2-carbonyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

Step 1: Preparation of tert-butyl (R)-2-(4-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-V)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperazine-1-carbonyl)-2-methylpyrrolidine-1-carboxylate. A mixture of 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile dihydrochloride (Example 8; 50 mg, 0.11 mmol), R-1-(tert-butoxycarbonyl)-2-methylpyrrolidine-2-carboxylic acid (25 mg, 0.11 mmol) and HATU (124 mg, 0.33 mmol) in anhydrous DCM (545 μL) was treated with DIEA (19 μL, 0.11 mmol). The resulting mixture was stirred overnight at ambient temperature. The reaction mixture was filtered, and the filtrate was concentrated in vacuo. The residue was purified by silica chromatography (using 0-20% DCM:MeOH with 0-2% NH₄OH as the gradient eluent). Fractions containing the desired product were combined, concentrated and triturated with DCM/Hexanes (1:10) to afford the title compound (65 mg, quantitative yield) which was used directly in Step 2. MS (apci) m/z=597.3 (M+H).

Step 2: Preparation of (R)-6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(4-(2-methylpyrrolidine-2-carbonyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile. A solution of tert-butyl (R)-2-(4-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperazine-1-carbonyl)-2-methylpyrrolidine-1-carboxylate (Step 1; 65 mg, 0.11 mmol) in 1:1 TFA:DCM (1.2 mL) was stirred 2 h at ambient temperature. The reaction mixture was quenched with saturated NaHCO_(3(aq)) and then washed with water and brine. The organic extracts were dried over anhydrous Na₂SO_(4(s)), filtered, and concentrated in vacuo. The residue was purified by C18 reverse phase chromatography (using 5-95% water:ACN with 0.1% TFA as the gradient eluent). Fractions containing the desired product were combined and re-purified using silica chromatography (0-20% DCM:MeOH with 0-2% NH₄OH as the gradient eluent). The fractions containing the desired compound were combined and concentrated in vacuo. The residue was triturated with DCM/Hexanes 1:10) and dried in vacuo to cleanly afford the title compound (15 mg, 28% yield). MS (apci) m/z=497.3 (M+H).

Example 71

(S)-6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(4-(2-methylpyrrolidine-2-carbonyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

Step 1: Preparation of tert-butyl (S)-2-(4-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperazine-1-carbonyl)-2-methylpyrrolidine-1-carboxylate. A mixture of 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile dihydrochloride (Example 8; 50 mg, 0.11 mmol), (S)-1-(tert-butoxycarbonyl)-2-methylpyrrolidine-2-carboxylic acid (25 mg, 0.11 mmol) and HATU (124 mg, 0.33 mmol) in anhydrous DCM (545 μL) was treated with DIEA (76 μL, 0.44 mmol). After stirring the reaction mixture for 3 h at ambient temperature, DMF (1 mL) and additional DIEA (76 μL, 0.44 mmol) were added, and the resulting mixture was stirred for 24 h at ambient temperature. The reaction mixture was filtered, and the filtrate was concentrated in vacuo. The residue was purified by silica chromatography (using 0-20% DCM:MeOH with 0-1% NH₄OH as the gradient eluent). Fractions containing the desired product were combined, concentrated, triturated with DCM/Hexanes (1:10) and concentrated in vacuo to afford the title compound (65 mg, quantitative yield) which was used directly in Step 2. MS (apci) m/z=597.3 (M+H).

Step 2: Preparation of (S)-6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(4-(2-methylpyrrolidine-2-carbonyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile. A solution of tert-butyl (S)-2-(4-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperazine-1-carbonyl)-2-methylpyrrolidine-1-carboxylate (Step 1; 65 mg, 0.11 mmol) in DCM (1.1 mL) was treated with TFA (84 μL, 1.1 mmol), then stirred overnight at ambient temperature. The reaction mixture was concentrated in vacuo, and the residue was purified by C18 reverse phase chromatography (using 5-95% water: ACN with 0.1% TFA as the gradient eluent). Fractions containing the desired product were combined, diluted with 4:1 DCM:iPrOH and washed sequentially with saturated NaHCO_(3(aq)) and brine. The organic extracts were dried over anhydrous Na₂SO_(4(s)), filtered, and concentrated in vacuo. The residue was triturated with DCM/Hexanes (1:10) and dried in vacuo to cleanly afford the title compound (17 mg, 31% yield). MS (apci) m/z=497.3 (M+H).

Example 72

(R)-6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(4-(pyrrolidine-3-carbonyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

Step 1: Preparation of tert-butyl (R)-3-(4-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-VI)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperazine-1-carbonyl)pyrrolidine-1-carboxylate. A mixture of 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile dihydrochloride (Example 8; 195 mg, 0.425 mmol), (R)-1-(tert-butoxycarbonyl)pyrrolidine-3-carboxylic acid (91.6 mg, 0.425 mmol) and HATU (485 mg, 1.28 mmol) in anhydrous DCM (2.1 mL) was treated with DIEA (73.4 μL, 0.425 mmol). After stirring for 2 h at ambient temperature, the reaction mixture was filtered, and the filtrate was concentrated in vacuo. The residue was purified by silica chromatography (using (0-10% DCM:MeOH with 0-1% NH₄OH as the gradient eluent). Fractions containing the desired product were combined, concentrated and triturated with DCM/Hexanes (1:10) and dried in vacuo for 1 h to afford the title compound (248 mg, quantitative yield) which was used directly in Step 2. MS (apci) m/z=583.3 (M+H).

Step 2: Preparation of (R)-6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(4-(pyrrolidine-3-carbonyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile. A solution tert-butyl (R)-3-(4-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperazine-1-carbonyl)pyrrolidine-1-carboxylate (Step 1; 248 mg, 0.426 mmol) in DCM (4.3 mL) was treated with TFA (328 μL, 4.26 mmol), and stirred for 45 min at ambient temperature. Additional TFA (328 μL, 4.26 mmol) was introduced, and the reaction mixture was stirred overnight at ambient temperature. The reaction mixture was concentrated in vacuo, and the residue was purified by C18 reverse phase chromatography (using 5-95% water: ACN with 0.1% TFA as the gradient eluent). Fractions containing the desired product were combined, diluted with 4:1 DCM:iPrOH and washed sequentially with saturated NaHCO_(3(aq)) and brine. The combined organic extracts were dried over anhydrous Na₂SO_(4(s)), filtered, and concentrated in vacuo. The residue was triturated with DCM/Hexanes (1:10) and dried in vacuo to cleanly afford the title compound (39.1 mg, 19% yield). MS (apci) m/z=483.2 (M+H).

Example 73

(S)-6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(4-(pyrrolidine-3-carbonyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

Step 1: Preparation of tert-butyl (S)-3-(4-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-VI)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperazine-1-carbonyl)pyrrolidine-1-carboxylate. A mixture of 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile dihydrochloride (Example 8; 50 mg, 0.11 mmol), (S)-1-(tert-butoxycarbonyl)pyrrolidine-3-carboxylic acid (23 mg, 0.11 mmol) and HATU (124 mg, 0.33 mmol) in anhydrous DCM (545 μL) was treated with DIEA (76 μL, 0.44 mmol). After stirring for 3 h at ambient temperature, the reaction mixture was filtered, and the filtrate was concentrated in vacuo. The residue was purified by silica chromatography (using (0-20% DCM:MeOH with 0-1% NH₄OH as the gradient eluent). Fractions containing the desired product were combined, concentrated and triturated with DCM/Hexanes (1:10) and dried in vacuo for 1 h to afford the title compound (64 mg, quantitative yield) which was used directly in Step 2. MS (apci) m/z=583.3 (M+H).

Step 2: Preparation of (S)-6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(4-(pyrrolidine-3-carbonyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile. A solution tert-butyl (S)-3-(4-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperazine-1-carbonyl)pyrrolidine-1-carboxylate (Step 1; 64 mg, 0.11 mmol) in DCM (1.1 mL) was treated with TFA (85 μL, 1.1 mmol), then stirred for 1 h at ambient temperature. The reaction mixture was diluted with 4:1 DCM:iPrOH and washed sequentially with saturated NaHCO_(3(aq)) and brine. The combined organic extracts were dried over anhydrous Na₂SO_(4(s)), filtered, and concentrated in vacuo. The residue was triturated with DCM/Hexanes (1:10) and dried in vacuo to cleanly afford the title compound (48 mg, 91% yield). MS (apci) m/z=483.3 (M+H).

Example 74

6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(4-((trans-(±))-4-phenylpyrrolidine-3-carbonyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

Step 1: Preparation of tert-butyl-trans-(±)-3-(4-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperazine-1-carbonyl)-4-phenylpyrrolidine-1-carboxylate. A mixture of 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile dihydrochloride (Example 8; 200 mg, 0.436 mmol), trans-(±)-1-(tert-butoxycarbonyl)-4-phenylpyrrolidine-3-carboxylic acid (127 mg, 0.436 mmol) and HATU (498 mg, 1.31 mmol) in anhydrous DCM (2.2 mL) was treated with DIEA (76.2 μL, 0.436 mmol). After stirring for 3 h at ambient temperature, the reaction mixture was filtered, and the filtrate was concentrated in vacuo. The residue was purified by silica chromatography (using 0-20% DCM:MeOH as the gradient eluent). Fractions containing the desired product were combined, concentrated and triturated with DCM/Hexanes (1:10) and dried in vacuo for 1 h to afford the title compound (287 mg, quantitative yield) which was used directly in Step 2. MS (apci) m/z=659.3 (M+H). Step 2: Preparation of 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(4-(-trans-(±)-4-phenylpyrrolidine-3-carbonyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile. A solution of tert-butyl-trans-(±)-3-(4-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperazine-1-carbonyl)-4-phenylpyrrolidine-1-carboxylate (Step 1; 287 mg, 0.436 mmol) in DCM (4.4 mL) was treated with TFA (336 μL, 4.36 mmol) and stirred overnight at ambient temperature. The resulting mixture was concentrated in vacuo, and the residue was purified by C18 reverse phase chromatography (using 5-95% water: ACN with 0.1% TFA as the gradient eluent). Fractions containing the desired product were combined, diluted with 4:1 DCM:iPrOH and washed sequentially with saturated NaHCO_(3(aq)), water and brine. The combined organic extracts were dried over anhydrous Na₂SO_(4(s)), filtered, and concentrated in vacuo. The residue was triturated with DCM/Hexanes (1:10) and dried in vacuo overnight to cleanly afford the title compound (242 mg, 99% yield). MS (apci) m/z=559.3 (M+H).

Example 75

4-(6-(4-(D-leucyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

Step 1: Preparation of tert-butyl (R)-(1-(4-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperazin-1-yl)-4-methyl-1-oxopentan-2-yl)carbamate. A mixture of 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile dihydrochloride (Example 8; 55 mg, 0.120 mmol), HATU (54.8 mg, 0.144 mmol) and 2(tert-butoxycarbonyl)-D-leucine (30.5 mg, 0.132 mmol) in anhydrous DCM (4 mL) was treated with DIEA (83.6 μL, 0.480 mmol). The reaction mixture was stirred for 3 d at ambient temperature. The resulting mixture was purified by silica phase chromatography (using 30-100% ethyl acetate in hexanes as the gradient eluent) to afford the title compound (70 mg, 97% yield). MS (apci) m/z=599.3 (M+H).

Step 2: Preparation of 4-(6-(4-(D-leucyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile. A solution of tert-butyl (R)-(1-(4-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperazin-1-yl)-4-methyl-1-oxopentan-2-yl)carbamate (Step 1; 0.070 g, 0.12 mmol) was dissolved in DCM (4 mL) and treated with TFA (2 mL). The resulting mixture was stirred for 1 h at ambient temperature and then concentrated in vacuo. The residue was purified by C18 reverse phase chromatography (using 5-95% ACN in water with 0.1% TFA as the gradient eluent). Fractions containing the desired product were combined, diluted with 4:1 DCM:iPrOH and washed sequentially with saturated NaHCO_(3(aq)) and brine. The combined organic extracts were dried over anhydrous Na₂SO_(4(s)), filtered, and concentrated in vacuo to afford the title compound (43 mg, 74% yield). MS (apci) m/z=499.3 (M+H).

Example 76

(S)-4-(6-(4-(2-(aminomethyl)-4-methylpentanoyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

Step 1: Preparation of tert-butyl (S)-(2-(4-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperazine-1-carbonyl)-4-methylpentyl)carbamate. A mixture of 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile dihydrochloride (Example 8; 55 mg, 0.120 mmol), HATU (54.8 mg, 0.144 mmol) and (S)-2-(((tert-Butoxycarbonyl)amino)methyl)-4-methylpentanoic acid (32.4 mg, 0.132 mmol) in anhydrous DCM (4 mL) was treated with DIEA (83.6 μl, 0.480 mmol). The reaction mixture was stirred overnight at ambient temperature. The resulting mixture was concentrated in vacuo to afford the title compound in sufficient purity for subsequent use (73 mg, 99% yield). MS (apci) m/z=613.4 (M+H).

Step 2: Preparation of (S)-4-(6-(4-(2-(aminomethyl)-4-methylpentanoyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile. A solution of tert-butyl (S)-(2-(4-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperazine-1-carbonyl)-4-methylpentyl)carbamate (Step 1; 73 mg, 0.12 mmol) was dissolved in DCM (4 mL) and treated with TFA (2 mL). The resulting mixture was stirred for 30 min at ambient temperature and then concentrated in vacuo. The residue was purified by C18 reverse phase chromatography (using 5-95% ACN in water with 0.1% TFA as the gradient eluent). Fractions containing the desired product were combined, diluted with 4:1 DCM:iPrOH and washed sequentially with saturated NaHCO_(3(aq)) and brine. The combined organic extracts were dried over anhydrous Na₂SO_(4(s)), filtered, and concentrated in vacuo to afford the title compound (43 mg, 70% yield). MS (apci) m/z=513.2 (M+H).

Example 77

4-(6-(4-(2-(4-chlorophenyl)-2-(dimethylamino)acetyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

A solution of 4-(6-(4-(2-amino-2-(4-chlorophenyl)acetyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile (Example 61; 37 mg, 0.067 mmol) and formaldehyde (20 μL, 0.27 mmol) in dry DCM (669 μL) was treated with NaBH(AcO)₃ (132 mg, 0.502 mmol). The resulting mixture was stirred for 2 h at ambient temperature. The reaction mixture was filtered, and the filtrate was concentrated in vacuo. The residue was purified by C18 reverse phase chromatography (using 5-95% water: ACN with 0.1% TFA as the gradient eluent). Fractions containing the desired product were combined, diluted with 4:1 DCM:iPrOH and washed sequentially with saturated NaHCO_(3(aq)), water and brine. The combined organic extracts were dried over anhydrous Na₂SO_(4(s)), filtered, and concentrated in vacuo. The residue was triturated with DCM/Hexanes (1:10) and dried in vacuo to cleanly afford the title compound (27.2 mg, 70% yield). MS (apci) m/z=581.2 (M+H).

Example 78

4-(6-(4-(2-(3-chloro-4-fluorophenyl)-2-(dimethylamino)acetyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

A solution of 4-(6-(4-(2-amino-2-(3-chloro-4-fluorophenyl)acetyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile (Example 65; 152 mg, 0.266 mmol) and formaldehyde (79.3 μL, 1.06 mmol) in dry DCM (2.66 mL) was treated with NaBH(AcO)₃ (282 mg, 1.33 mmol). The resulting mixture was stirred overnight at ambient temperature. The reaction mixture was concentrated in vacuo, and the residue was purified by C18 reverse phase chromatography (using 5-95% water: ACN with 0.1% TFA as the gradient eluent). Fractions containing the desired product were combined, concentrated in vacuo, suspended in DCM and washed sequentially with saturated NaHCO_(3(aq)), water and brine. The combined organic extracts were dried over anhydrous Na₂SO_(4(s)), filtered, and concentrated in vacuo to cleanly afford the title compound (74.3 mg, 47% yield). MS (apci) m/z=599.2 (M+H).

Example 79

4-(6-(4-(2-(2,4-difluorophenyl)-2-(dimethylamino)acetyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

A solution of 4-(6-(4-(2-amino-2-(2,4-difluorophenyl)acetyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile (Example 64; 89 mg, 0.16 mmol) and formaldehyde (48 μL, 0.64 mmol) in dry DCM (1.6 mL) was treated with NaBH(AcO)₃ (170 mg, 0.802 mmol). The resulting mixture was stirred for 1 h at ambient temperature. The reaction mixture was concentrated in vacuo, and the residue was purified by C18 reverse phase chromatography (using 5-95% water: ACN with 0.1% TFA as the gradient eluent). Fractions containing the desired product were combined, diluted with 4:1 DCM:iPrOH, and washed sequentially with saturated NaHCO_(3(aq)) and brine. The combined organic extracts were dried over anhydrous Na₂SO_(4(s)), filtered, and concentrated in vacuo. The residue was triturated with DCM/Hexanes (1:10) and dried overnight in vacuo to cleanly afford the title compound (56.2 mg, 60% yield). MS (apci) m/z=583.3 (M+H).

The compounds in Table F were prepared and purified using a similar method to that described for the synthesis of Example 79, replacing 4-(6-(4-(2-amino-2-(2,4-difluorophenyl)acetyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile with the appropriate amine (source noted in table). Reactions were monitored for completion by LCMS, and reaction durations, and where noted, quantities of formaldehyde and NaBH(AcO)₃, were adjusted accordingly. The title compounds were cleanly isolated following a similar C18 reverse phase chromatography using an appropriate gradient and free basing extraction sequence to that used in the synthesis of Example 79.

TABLE F MS Starting (apci) Ex. # material Structure Chemical Name m/z 80 Ex. 63

4-(6-(4-(2- (dimethylamino)-2-(2- fluorophenyl)acetyl) piperazin-1-yl)pyridin-3- yl)-6-(1-methyl-1H- pyrazol-4- yl)pyrazolo[1,5- a]pyrazine-3-carbonitrile 565.30 (M + H) 81 Ex. 66

(R)-4-(6-(4-(2- (dimethylamino)-2- phenylpropanoyl) piperazin-1-yl)pyridin- 3-yl)-6- (1-methyl-1H-pyrazol-4- yl)pyrazolo[1,5- a]pyrazine-3-carbonitrile 561.30 (M + H) 82 Ex. 68

4-(6-(4-(3- (dimethylamino)-2-(4- fluorophenyl)propanoyl) piperazin-1-yl)pyridin-3- yl)-6-(1-methyl-1H- pyrazol-4- yl)pyrazolo[1,5- a]pyrazine-3-carbonitrile 579.30 (M + H) 83 Ex. 69

6-(1-methyl-1H-pyrazol- 4-yl)-4-(6-(4-((2S)-2-(1- methylpyrrolidin-2-yl)-2- phenylacetyl)piperazin- 1-yl)pyridin-3- yl)pyrazolo[1,5- a]pyrazine-3-carbonitrile 587.30 (M + H) 84 Ex. 70

(R)-4-(6-(4-(1,2- dimethylpyrrolidine-2- carbonyl)piperazin-1- yl)pyridin-3-yl)-6-(1- methyl-1H-pyrazol-4- yl)pyrazolo[1,5- a]pyrazine-3-carbonitrile 511.30 (M + H) 85 Ex. 71

(S)-4-(6-(4-(1,2- dimethylpyrrolidine-2- carbonyl)piperazin-1- yl)pyridin-3-yl)-6-(1- methyl-1H-pyrazol-4- yl)pyrazolo[1,5- a]pyrazine-3-carbonitrile 511.30 (M + H) 86 Ex. 72

(R)-6-(1-methyl-1H- pyrazol-4-yl)-4-(6-(4-(1- methylpyrrolidine-3- carbonyl)piperazin-1- yl)pyridin-3- yl)pyrazolo[1,5- a]pyrazine-3-carbonitrile 497.30 (M + H) 87 Ex. 73

(S)-6-(1-methyl-1H- pyrazol-4-yl)-4-(6-(4-(1- methylpyrrolidine-3- carbonyl)piperazin-1- yl)pyridin-3- yl)pyrazolo[1,5- a]pyrazine-3-carbonitrile 497.30 (M + H) 88 Ex. 74

6-(1-methyl-1H-pyrazol- 4-yl)-4-(6-(4-((trans-(±))- 4-phenylpyrrolidine-3- carbonyl)piperazin-1- yl)pyridin-3- yl)pyrazolo[1,5- a]pyrazine-3-carbonitrile 573.20 (M + H) *10 equivalents of formaldehyde and 5 equivalents of NaBH(AcO)₃ were used in this reaction **5 equivalents of formaldehyde and 5 equivalents of NaBH(AcO)₃ were used in this reaction; trituration was skipped in this example

Examples 89 and 90 6-(1-methyl-IH-pyrazol-4-yl)-4-(6-(4-((3S,4R)-1-methyl-4-phenylpyrrolidine-3-carbonyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile (Ex. 89) and 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(4-((3R,4S)-1-methyl-4-phenylpyrrolidine-3-carbonyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile (Ex. 90)

A solution of the racemate 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(4-((trans-(±))-4-phenylpyrrolidine-3-carbonyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile (Ex. 88; 142 mg, 0.25 mmol) was separated into the respective enantiomers by Super-Critical Fluid Chromatography (SFC) utilizing an isocratic mobile phase consisting of A: 28% (Methanol:Isopropyl alcohol:diethylamine [80:20:1]) and B: 72% (super critical Carbon Dioxide), with a flow rate of 4 mL/min. achieved upon a stationary phase OD-H column (Chiral Technology, Inc.; cellulose—α-D 1-4 Glucose(tris[3,5-dimethylphenylcarbamate]); 4.6 mm×250 mm, 5 u). Injections and chromatography were monitored with fixed wavelength UV @ 220 nm and 254 nm. Fractions containing each enantiomer were isolated and independently concentrated in vacuo to cleanly afford the two title compounds: Peak 1, Example 89: 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(4-((3S,4R)-1-methyl-4-phenylpyrrolidine-3-carbonyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile. MS (apci) m/z=572.3 (M+H). Peak 2, Example 90: 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(4-((3R,4S)-1-methyl-4-phenylpyrrolidine-3-carbonyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile. MS (apci) m/z=572.3 (M+H).

Example 91

(R)-4-(6-(4-(3-(dimethylamino)-2-phenylpropanoyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

A solution of (R)-4-(6-(4-(3-amino-2-phenylpropanoyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile (Example 67; 43 mg, 0.081 mmol) and formaldehyde (22 μL, 0.81 mmol) in dry DCM (0.81 mL) was treated with NaBH(AcO)₃ (86 mg, 0.40 mmol). After stirring the mixture overnight additional formaldehyde (22 μL, 0.81 mmol) and NaBH(AcO)₃ (86 mg, 0.40 mmol) were added, and the reaction was again allowed to stir overnight at ambient temperature. The reaction mixture was purified by silica chromatography (using 0-10% CHCl₃:MeOH with 0-1% NH₄OH as the gradient eluent). Fractions containing the desired product were combined, concentrated in vacuo, and triturated with DCM/Hexanes (1:10) to cleanly afford the title compound (11.6 mg, 26% yield). MS (apci) m/z=561.3 (M+H).

Example 92

(4-(6-(4-(2-(dimethylamino)-2-(4-fluorophenyl)acetyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

The title compound was prepared and purified using a similar procedure to that described for Example 91, replacing (R)-4-(6-(4-(3-amino-2-phenylpropanoyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile with (R)-4-(6-(4-(2-amino-2-(4-fluorophenyl)acetyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile (Example 62). MS (apci) m/z=565.3 (M+H).

Example 93

4-(6-(4-(2-(3-chlorophenyl)-2-(dimethylamino)acetyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

A solution of 4-(6-(4-(2-amino-2-(3-chlorophenyl)acetyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile (Example 60; 430 mg, 0.778 mmol) and formaldehyde (232 μL, 3.11 mmol) in 1:1 DCM:MeOH (8 mL) was treated with NaBH(AcO)₃ (824 mg, 3.89 mmol). After stirring the mixture overnight at ambient temperature, the resulting suspension was filtered, and the filtrate was concentrated in vacuo. The residue was subsequently purified by C18 reverse phase chromatography (using 5-95% water:ACN as the gradient eluent). Fractions containing the desired product were combined, concentrated in vacuo, and triturated with DCM/Hexanes (1:10) then dried again in vacuo for 5 d to cleanly afford the title compound (154 mg, 34% yield). MS (apci) m/z=581.2 (M+H).

Examples 94 and 95 (R)-4-(6-(4-(2-(3-chlorophenyl)-2-(dimethylamino)acetyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile (Ex. 94) and (S)-4-(6-(4-(2-(3-chlorophenyl)-2-(dimethylamino)acetyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile (Ex. 95)

A solution of the racemate 4-(6-(4-(2-(3-chlorophenyl)-2-(dim ethyl amino)acetyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile (Example 93; 147 mg, 0.260 mmol) was separated into the respective enantiomers by Super-Critical Fluid Chromatography (SFC) utilizing an isocratic mobile phase consisting of A: 28% (Methanol:Isopropyl alcohol:diethylamine [80:20:1]) and B: 72% (super critical Carbon Dioxide), with a flow rate of 4 mL/min. achieved upon a stationary phase (Chiral Technology, Inc., OD-H column (cellulose—α-D 1-4 Glucose(tris[3,5-dimethylphenylcarbamate]), 4.6 mm×250 mm, 5 u). Injections and chromatography were monitored with fixed wavelength UV @ 220 nm and 254 nm.

Fractions containing the enantiomer in Peak 1 were isolated and independently concentrated in vacuo to provide Example 94: (R)-4-(6-(4-(2-(3-chlorophenyl)-2-(dimethyl amino)acetyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile (14.1 mg, 10% recovery). MS (apci) m/z=581.3 (M+H). 1H NMR (400 MHz, CDCl₃) δ 8.76 (d, J=1.9 Hz, 1H), 8.52 (s, 1H), 8.33 (s, 1H), 8.05 (dd, J=8.9, 2.5 Hz, 1H), 7.96 (d, J=6.9 Hz, 2H), 7.47 (s, 1H), 7.37-7.28 (m, 3H), 6.73 (d, J=8.5 Hz, 1H), 4.22 (s, 1H), 3.98 (s, 3H), 3.71 (m, 7H), 3.41 (m, 1H), 2.32 (s, 6H).

Fractions containing the enantiomer in Peak 2 were combined, concentrated in vacuo but found to be impure. This material was re-purified by C18 reverse phase chromatography (using 5-95% water: ACN with 0.1% TFA as the gradient eluent). Fractions containing the desired product were combined, diluted with 4:1 DCM:iPrOH and washed sequentially with saturated NaHCO_(3(aq)) and brine. The organic extracts were dried over anhydrous Na₂SO_(4(s)), filtered, and concentrated in vacuo. The residue was triturated with DCM/Hexanes (1:10) and dried overnight in vacuo to cleanly afford Example 95: (S)-4-(6-(4-(2-(3-chlorophenyl)-2-(dimethylamino)acetyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile (12.7 mg, 9% recovery). MS (apci) m/z=581.3 (M+H).

Example 96

4-(6-(4-(dimethyl-D-leucyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

A solution of 4-(6-(4-(D-leucyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile (Example 75; 37.4 mg, 0.0750 mmol) and formaldehyde (55.8 μL, 0.750 mmol) in DCM (750 μL) was treated with NaBH(AcO)₃ (79.5 mg, 0.375 mmol). After stirring the mixture 3 h at ambient temperature, the reaction mixture was concentrated in vacuo. The residue was subsequently purified by C18 reverse phase chromatography (using 5-95% water:ACN with 0.1% TFA as the gradient eluent). Fractions containing the desired product were combined, diluted with 4:1 DCM:iPrOH and washed sequentially with saturated NaHCO_(3(aq)) and brine. The organic extracts were dried over anhydrous Na₂SO_(4(s)), filtered, and concentrated in vacuo to afford the title compound (21 mg, 53% yield). MS (apci) m/z=527.3 (M+H).

Example 97

(S)-4-(6-(4-(2-((dimethylamino)methyl)-4-methylpentanoyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

The title compound was prepared and purified using a similar procedure to that described for Example 96, replacing 4-(6-(4-(D-leucyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile (Example 75), with (S)-4-(6-(4-(2-(aminomethyl)-4-methylpentanoyl)piperazin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile (Example 76). MS (apci) m/z=541.3 (M+H).

Example 98

6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(4-(pyridin-2-yloxy)piperidin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

A solution of 4-(6-fluoropyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile (Intermediate P7; 52.3 mg, 0.208 mmol) in DMSO (1 mL) was treated with 2-(piperidin-4-yloxy)pyridine dihydrochloride (79 mg, 0.78 mmol) and Cs₂CO_(3(s)) (280 mg, 0.858 mmol) then stirred overnight at 60° C. After cooling to ambient temperature, the reaction mixture was diluted with water, and extracted with DCM (4×). The combined organic extracts were washed with water, then dried over anhydrous Na₂SO_(4(s)), filtered, and concentrated in vacuo. The residue was purified by silica chromatography (using 0-100% Hexanes/EtOAc as the gradient eluent) to afford the title compound (19.7 mg, 39% yield). MS (apci) m/z=478.2 (M+H).

Example 99

6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(4-((6-methylpyridazin-3-yl)oxy)piperidin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

A solution of 4-(6-fluoropyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile (Intermediate P7; 26.1 mg, 0.0817 mmol) in DMSO (1 mL) was treated with 3-methyl-6-(piperidin-4-yloxy)pyridazine (Intermediate R6; 39.6 mg, 0.205 mmol) and Cs₂CO_(3(s)) (266 mg, 0.817 mmol) then stirred overnight at 60° C. After cooling to ambient temperature, the reaction mixture was diluted with water, and extracted with DCM (4×). The combined organic extracts were washed with water, then dried over anhydrous Na₂SO_(4(s)), filtered, and concentrated in vacuo. The residue was purified by silica chromatography (using 0-100% Hexanes/EtOAc as the gradient eluent) to afford the title compound (15.5 mg, 33% yield). MS (apci) m/z=493.2 (M+H).

Example 100

4-(6-(4-((6-methoxypyridazin-3-yl)oxy)piperidin-1-yl)pyridin-3-yl)-6-(1-methyl 1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

A solution of 4-(6-fluoropyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile (Intermediate P7; 25.3 mg, 0.0792 mmol) in DMSO (1 mL) was treated with 3-methoxy-6-(piperidin-4-yloxy)pyridazine (Intermediate R7; 33.2 mg, 0.159 mmol) and Cs₂CO_(3(s)) (258 mg, 0.792 mmol) then stirred overnight at 60° C. After cooling to ambient temperature, the reaction mixture was diluted with water and extracted with DCM (4×). The combined organic extracts were washed with water, then dried over anhydrous Na₂SO_(4(s)), filtered, and concentrated in vacuo. The residue was purified by silica chromatography (using 0-100% Hexanes/EtOAc as the gradient eluent) to afford the title compound (1.9 mg, 4.7% yield). MS (apci) m/z=509.2 (M+H).

Example 101

4-(6-(4-benzyl-4-hydroxypiperidin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

A solution of 4-(6-fluoropyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile (Intermediate P7; 28.5 mg, 0.0893 mmol) in DMSO (0.5 mL) was treated with 4-benzylpiperidin-4-ol (51.2 mg, 0.268 mmol) and Cs₂CO_(3(s)) (174 mg, 0.536 mmol) then stirred overnight at 60° C. The reaction mixture was diluted with water, and extracted with DCM (3×). The combined organic extracts were dried over anhydrous Na₂SO_(4(s)), filtered, and concentrated in vacuo. The residue was purified by silica chromatography (using 0-100% Hexanes/EtOAc as the gradient eluent) to afford the title compound (11.7 mg, 27% yield). MS (apci) m/z=491.2 (M+H).

Example 102

4-(6-(4-hydroxy-4-(pyridin-2-ylmethyl)piperidin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

A solution of 4-(6-fluoropyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile (Intermediate P7; 35.6 mg, 0.111 mmol) in DMSO (0.5 mL) was treated with 4-(pyridin-2-ylmethyl)piperidin-4-ol (64.3 mg, 0.334 mmol) and Cs₂CO_(3(s)) (218 mg, 0.669 mmol) then stirred overnight at 60° C. After cooling to ambient temperature, the reaction mixture was diluted with water and extracted with DCM (3×). The combined organic extracts were dried over anhydrous Na₂SO_(4(s)), filtered, and concentrated in vacuo. The residue was purified by silica chromatography (using 0-100% Hexanes/EtOAc as the gradient eluent) to afford the title compound (29.8 mg, 45% yield). MS (apci) m/z=492.2 (M+H).

Example 103

tert-butyl (R)-(1-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperidin-3-yl)carbamate

A solution of 4-(6-fluoropyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile (Intermediate P7; 69 mg, 0.20 mmol) in DMA (10 mL) was treated with tert-butyl (R)-piperidin-3-ylcarbamate (122 mg, 0.609 mmol) and TEA (142 μL, 1.02 mmol) then stirred 4 h at 60° C. After cooling to ambient temperature, the reaction mixture was purified by silica chromatography (using 0-100% Hexanes/EtOAc as the gradient eluent) to afford the title compound (38.9 mg, 36% yield). MS (apci) m/z=500.2 (M+H).

Example 104

(R)-4-(6-(3-aminopiperidin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile 2,2,2-trifluoroacetate

A solution of tert-butyl (R)-(1-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperidin-3-yl)carbamate (Example 103; 23.7 mg, 0.0474 mmol) in DCM (47.4 μL) was treated dropwise with TFA (36.5 μL, 0.474 mmol). The resulting mixture was stirred for 1 h at ambient temperature and then concentrated in vacuo overnight to afford the title compound as the TFA salt (43 mg, 74% yield). MS (apci) m/z=400.1 (M+H).

Example 105

tert-butyl (S)-(1-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperidin-3-yl)carbamate

A solution of 4-(6-fluoropyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile (Intermediate P7; 64 mg, 0.18 mmol) in DMA (10 mL) was treated with tert-butyl (S)-piperidin-3-ylcarbamate (111 mg, 0.553 mmol) and TEA (129 μL, 0.922 mmol) and stirred for 4 h at 60° C. After cooling to ambient temperature, the reaction mixture was purified by silica chromatography (using 0-100% Hexanes/EtOAc as the gradient eluent) to afford the title compound (74.3 mg, 77% yield). MS (apci) m/z=500.2 (M+H).

Example 106

(S)-4-(6-(3-aminopiperidin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile 2,2,2-trifluoroacetate

A solution of tert-butyl (S)-(1-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperidin-3-yl)carbamate (Example 105; 42.8 mg, 0.0857 mmol) in DCM (85.7 μL) was treated dropwise with TFA (66.0 μL, 0.857 mmol). The resulting mixture was stirred for 1 h at ambient temperature and then concentrated in vacuo overnight to afford the title compound as the TFA salt (43 mg, 74% yield). MS (apci) m/z=400.0 (M+H).

Example 107

tert-butyl (1-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)-4-methylpiperidin-4-yl)carbamate

A solution of 4-(6-fluoropyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile (Intermediate P7; 252.1 mg, 0.7895 mmol) in DMSO (1 mL) was treated with 4-(pyridin-2-ylmethyl)piperidin-4-ol (64.3 mg, 0.334 mmol) and Cs₂CO_(3(s)) (1.80 g, 5.53 mmol) then stirred overnight at 60° C. After cooling to ambient temperature, the reaction mixture was diluted with water, and extracted with DCM (4×). The combined organic extracts were dried over anhydrous Na₂SO_(4(s)), filtered, and concentrated in vacuo. The residue was purified by silica chromatography (using 0-100% Hexanes/EtOAc as the gradient eluent) to afford the title compound (271.8 mg, 62% yield). MS (apci) m/z=514.2 (M+H).

Example 108

4-(6-(4-amino-4-methylpiperidin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

A solution of tert-butyl (1-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)-4-methylpiperidin-4-yl)carbamate (Example 105; 250 mg, 0.487 mmol) in DCM (4 mL) and treated with TFA (4 mL, 0.487 mmol). The reaction mixture was stirred for 4 d at ambient temperature and then concentrated in vacuo. The residue was dissolved in DCM and washed with saturated NaHCO_(3(aq)). The aqueous extracts were extracted with DCM. The combined organic extracts were dried over anhydrous Na₂SO_(4(s)), filtered, and concentrated in vacuo to afford the title compound (25.9 mg, 12% yield). MS (apci) m/z=414.2 (M+H).

Example 109

isopropyl (1-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)-4-methylpiperidin-4-yl)carbamate

A solution of 4-(6-(4-amino-4-methylpiperidin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile (Example 108; 6.5 mg, 0.016 mmol) and DIEA (4.06 mg, 0.0314 mmol) was dissolved in DCM (500 μL) and treated with isopropyl carbonochloridate (2.31 mg, 0.0189 mmol). The reaction mixture was stirred overnight at ambient temperature. The residue was treated with iPrOH and stirred at 60° C. for 3 h. The reaction mixture was cooled to ambient temperature, concentrated in vacuo and purified by silica chromatography (using 0-100% Hexanes/EtOAc as the gradient eluent) to afford the title compound (5.3 mg, 68% yield). MS (apci) m/z=500.2 (M+H).

Example 110

4-(6-(4-aminopiperidin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

Step 1: Preparation of tert-butyl (1-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperidin-4-yl)carbamate. A solution of 4-(6-fluoropyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile (Intermediate P7; 0.1054 g, 0.3301 mmol) in DMSO (6.6 mL) was treated with tert-butyl piperidin-4-ylcarbamate (0.2644 g, 1.320 mmol) and K₂CO_(3(s)) (0.1825 g, 1.320 mmol) then stirred 3 d at 110° C. After cooling to ambient temperature, the reaction mixture was diluted with water (10 mL), and extracted with DCM (2×20 mL). The combined organic extracts were dried over anhydrous MgSO_(4(s)), filtered, and concentrated in vacuo. The residue was purified by silica chromatography (using 0-100% EtOAc/Hexanes as the gradient eluent). Fractions containing the desired product were concentrated in vacuo, then suspended in water (to remove residual DMSO), filtered and dried in vacuo to afford the title compound (115.2 mg, 70% yield). MS (apci) m/z=500.3 (M+H).

Step 2: Preparation of 4-(6-(4-aminopiperidin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile. A solution of tert-butyl (1-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperidin-4-yl)carbamate (Step 1; 0.1152 g, 0.2306 mmol) was dissolved in CHCl₃ (3.1 mL) and treated with 5 M HCl in iPrOH (0.23 mL, 1.2 mmol). The reaction mixture was stirred for 8 h at ambient temperature and then concentrated in vacuo. The residue was dissolved in DCM and washed with saturated Na₂CO_(3(aq)). The aqueous extracts were extracted with DCM (2×40 mL). The combined organic extracts were dried over anhydrous MgSO_(4(s)), filtered, and concentrated in vacuo to afford the title compound (20 mg, 22% yield). MS (apci) m/z=400.2 (M+H).

Example 111

(S)-4-(6-(3-(aminomethyl)piperidin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile dihydrochloride

Step 1: Preparation of tert-butyl (S)-((1-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperidin-3-yl)methyl)carbamate. A solution of 4-(6-fluoropyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile (Intermediate P7; 0.1007 g, 0.3154 mmol) in DMSO (6.3 mL) was treated with tert-butyl (R)-(piperidin-3-ylmethyl)carbamate (0.2703 g, 1.261 mmol) and K₂CO_(3(s)) (0.1743 g, 1.261 mmol) and stirred for 30 min at 110° C. After cooling to ambient temperature, the reaction mixture was diluted with water (50 mL) and stirred for 1 h before filtering to afford the title compound (0.1527 mg, 94% yield). MS (apci) m/z=514.3 (M+H).

Step 2: Preparation of (S)-4-(6-(3-(aminomethyl)piperidin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile dihydrochloride. A solution of tert-butyl (S)-((1-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperidin-3-yl)methyl)carbamate (Step 1; 0.1527 g, 0.2973 mmol) was dissolved in CHCl₃ (4.0 mL) and treated with 5 M HCl in iPrOH (0.30 mL, 1.5 mmol). The resulting mixture was stirred 4 h at ambient temperature and then concentrated in vacuo to afford the title compound (0.1633 g, quantitative yield). MS (apci) m/z=414.2 (M+H).

Example 112

(R)-4-(6-(3-(aminomethyl)piperidin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile dihydrochloride

Step 1: Preparation of tert-butyl (R)-((1-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-VI)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperidin-3-yl)methyl)carbamate. A solution of 4-(6-fluoropyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile (Intermediate P7; 0.1003 g, 0.3141 mmol) in DMSO (6.3 mL) was treated with tert-butyl (S)-(piperidin-3-ylmethyl)carbamate (0.2693 g, 1.256 mmol) and K₂CO_(3(s)) (0.1737 g, 1.256 mmol) then stirred 30 min at 110° C. After cooling to ambient temperature, the reaction mixture was diluted with water (50 mL), and stirred for 1 h before filtering to afford the title compound (0.1381 mg, 86% yield). MS (apci) m/z=514.3 (M+H).

Step 2: Preparation of (R)-4-(6-(3-(aminomethyl)piperidin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile dihydrochloride. A solution of tert-butyl (R)-((1-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)piperidin-3-yl)methyl)carbamate (Step 1; 0.1381 g, 0.2689 mmol) was dissolved in CHCl₃ (3.6 mL) and treated with 5 M HCl in iPrOH (0.27 mL, 1.3 mmol). The resulting mixture was stirred 4 h at ambient temperature and then concentrated in vacuo to afford the title compound (0.1425 g, quantitative yield). MS (apci) m/z=414.2 (M+H).

Example 113

N-(1-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)-3-methylpiperidin-3-yl)acetamide hydrochloride

Step 1: Preparation of N-(1-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)-3-methylpiperidin-3-yl)acetamide. A solution of 4-(6-fluoropyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile (Intermediate P7; 0.0.035 g, 0.110 mmol) in DMSO (2.19 mL) was treated with N-(3-methylpiperidin-3-yl)acetamide 2,2,2-trifluoroacetate (Intermediate R8; 68.5 mg, 0.438 mmol) and K₂CO_(3(s)) (0.0606 g, 0.438 mmol) and stirred overnight at 110° C. After cooling to ambient temperature, the reaction mixture was diluted with water (50 mL), and stirred for 1 h before filtering to afford the title compound (0.0432 mg, 87% yield). MS (apci) m/z=456.2 (M+H).

Step 2: Preparation of N-(1-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)-3-methylpiperidin-3-yl)acetamide hydrochloride. A solution of N-(1-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)-3-methylpiperidin-3-yl)acetamide (Step 1; 0.0432 g, 0.0948 mmol) was dissolved in CHCl₃ (1.3 mL), and treated with 5 M HCl in iPrOH (0.09 mL, 0.47 mmol). The resulting mixture was stirred 4 h at ambient temperature and then concentrated in vacuo to afford the title compound (0.043 g, 75% yield). MS (apci) m/z=456.2 (M+H).

Example 114

(R)-4-(6-(3-(aminomethyl)pyrrolidin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

Step 1: Preparation of tert-butyl (R)-((1-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-ylpyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)pyrrolidin-3-yl)methyl)carbamate. A solution of 4-(6-fluoropyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile (Intermediate P7; 0.1019 g, 0.3191 mmol) in DMSO (6.4 mL) was treated with tert-butyl (S)-(pyrrolidin-3-ylmethyl)carbamate (0.2557 g, 1.277 mmol) and K₂CO_(3(s)) (0.1767 g, 1.277 mmol) and stirred 3 d at 110° C. After cooling to ambient temperature, the reaction mixture was diluted with water (10 mL), and extracted with DCM (2×20 mL). The combined organic extracts were dried over anhydrous MgSO_(4(s)), filtered, and concentrated in vacuo. The residue was purified by silica chromatography (using 0-100% EtOAc/Hexanes as the gradient eluent). Fractions containing the desired product were concentrated in vacuo, then suspended in water (to remove residual DMSO), filtered and dried in vacuo to afford the title compound (67 mg, 42% yield). MS (apci) m/z=500.2 (M+H).

Step 2: Preparation of (R)-4-(6-(3-(aminomethyl)pyrrolidin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile. A solution of tert-butyl (R)-((1-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)pyrrolidin-3-yl)methyl)carbamate (Step 1; 0.1019 g, 0.2040 mmol) was dissolved in CHCl₃ (2.7 mL) and treated with 5 M HCl in iPrOH (0.20 mL, 1.0 mmol). The reaction mixture was stirred 4 h at ambient temperature and then concentrated in vacuo. The residue was dissolved in DCM then washed with saturated Na₂CO_(3(aq)). The aqueous extracts were extracted with DCM (2×40 mL). The combined organic extracts were dried over anhydrous MgSO_(4(s)), filtered, and concentrated in vacuo to afford the title compound (5.7 mg, 7% yield). MS (apci) m/z=400.2 (M+H).

Example 115

(S)-4-(6-(3-(aminomethyl)pyrrolidin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

Step 1: Preparation of tert-butyl (S)-((1-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-ylpyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)pyrrolidin-3-yl)methyl)carbamate. A solution of 4-(6-fluoropyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile (Intermediate P7; 0.1020 g, 0.3194 mmol) in DMSO (6.4 mL) was treated with tert-butyl (R)-(pyrrolidin-3-ylmethyl)carbamate (0.2559 g, 1.278 mmol) and K₂CO_(3(s)) (0.1766 g, 1.278 mmol) then stirred 3 d at 110° C. After cooling to ambient temperature, the reaction mixture was diluted with water (10 mL), and extracted with DCM (2×20 mL). The combined organic extracts were dried over anhydrous MgSO_(4(s)), filtered, and concentrated in vacuo. The residue was purified by silica chromatography (using 0-100% EtOAc/Hexanes as the gradient eluent). Fractions containing the desired product were concentrated in vacuo, then suspended in water (to remove residual DMSO), filtered and dried in vacuo to afford the title compound (76.7 mg, 48% yield). MS (apci) m/z=500.2 (M+H).

Step 2: Preparation of (S)-4-(6-(3-(aminomethyl)pyrrolidin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile. A solution of tert-butyl (S)-((1-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)pyrrolidin-3-yl)methyl)carbamate (Step 1; 0.0767 g, 0.1535 mmol) was dissolved in CHCl₃ (2.0 mL) and treated with 5 M HCl in iPrOH (0.15 mL, 0.77 mmol). The reaction mixture was stirred 4 h at ambient temperature and then concentrated in vacuo. The residue was dissolved in DCM then washed with saturated Na₂CO_(3(aq)). The aqueous extracts were extracted with DCM (2×40 mL). The combined organic extracts were dried over anhydrous MgSO_(4(s)), filtered, and concentrated in vacuo to afford the title compound (18.9 mg, 31% yield). MS (apci) m/z=400.2 (M+H).

Example 116

4-(6-(3-(aminomethyl)azetidin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

Step 1: Preparation of tert-butyl ((1-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-VI)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)azetidin-3-yl)methyl)carbamate. A solution of 4-(6-fluoropyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile (Intermediate P7; 0.1014 g, 0.3176 mmol) in DMSO (6.4 mL) was treated with tert-butyl (azetidin-3-ylmethyl)carbamate (0.2366 g, 1.270 mmol) and K₂CO_(3(s)) (0.1756 g, 1.270 mmol) and stirred 3 d at 110° C. After cooling to ambient temperature, the reaction mixture was diluted with water (10 mL), and extracted with DCM (2×20 mL). The combined organic extracts were dried over anhydrous MgSO_(4(s)), filtered, and concentrated in vacuo. The residue was purified by silica chromatography (using 0-100% EtOAc/Hexanes as the gradient eluent). Fractions containing the desired product were concentrated in vacuo, then suspended in water (to remove residual DMSO), filtered and dried in vacuo to afford the title compound (97.1 mg, 63% yield). MS (apci) m/z=486.3 (M+H).

Step 2: Preparation of 4-(6-(3-(aminomethyl)azetidin-1-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile. A solution of tert-butyl ((1-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)azetidin-3-yl)methyl)carbamate (Step 1; 97 mg, 0.2 mmol) was dissolved in CHCl₃ (2.9 mL) and treated with 5 M HCl in iPrOH (0.21 mL, 1.1 mmol). The reaction mixture was stirred 4 h at ambient temperature and then concentrated in vacuo. The residue was dissolved in DCM and washed with saturated Na₂CO_(3(aq)). The aqueous extracts were extracted with DCM (2×40 mL). The combined organic extracts were dried over anhydrous MgSO_(4(s)), filtered, and concentrated in vacuo to afford the title compound (82.6 mg, 13% yield). MS (apci) m/z=386.2 (M+H).

Example 117

4-(6-(3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile dihydrochloride

Step 1: Preparation of tert-butyl 3-(5-(3-cyano-6-(1-methyl-IH-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)-3,6-diazabicyclo[3.1.1]heptane-6-carboxylate. In a pressure vessel, a mixture of 4-chloro-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile (Intermediate P2; 0.045 g, 0.17 mmol) and (6-(6-(tert-butoxycarbonyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)boronic acid (Intermediate R11; 0.06 g, 0.19 mmol) in 1,4-dioxane (2 mL) and 2 N Na₂CO_(3(aq)) (0.75 mL, 1.0 mmol) was treated with Pd(PPh₃)₄ (6 mg, 0.005 mmol) and sparged with N_(2(g)) for 15 min. The vessel was sealed and mixture was stirred overnight at 90° C. After cooling to ambient temperature, the mixture was diluted with water (3 mL) and DCM (8 mL), then stirred for 2 h at ambient temperature. The resulting biphasic mixture was extracted with additional DCM (3×) and the combined organic extracts were dried over anhydrous MgSO_(4(s)), filtered, and concentrated in vacuo. The residue was suspended in Et₂O (20 mL), and the suspension was stirred for 30 min at ambient temperature. The slurry was filtered, and the solids were dissolved in DCM for purification by silica chromatography (using 50-100% EtOAc/Hexanes as the gradient eluent) to cleanly afford the title compound (30 mg, 35% yield). MS (apci) m/z=498.2 (M+H).

Step 2: Preparation of 6-(1-methyl-1H-pyrazol-4-yl)-4-(6-(piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile. A solution of tert-butyl 3-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)-3,6-diazabicyclo[3.1.1]heptane-6-carboxylate (Step 1; 30 mg, 0.060 mmol) in DCM (5 mL) was treated with 5 M HCl in iPrOH (0.1 mL, 0.30 mmol) and stirred overnight at ambient temperature. The resulting mixture was concentrated in vacuo to cleanly afford the title compound (33 mg, quantitative yield). MS (apci) m/z=398.2 (M+H).

Example 118

4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

A solution of 4-(6-(3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile dihydrochloride (Example 117; 30 mg, 0.064 mmol) in DMA (1 mL) was treated sequentially with 6-methoxynicotinaldehyde (13 mg, 0.096 mmol) and NaBH(AcO)₃ (20 mg, 0.096 mmol). After stirring the mixture for 3 d at ambient temperature, additional 6-methoxynicotinaldehyde (8.7 mg, 0.064 mmol) and NaBH(AcO)₃ (13.3 mg, 0.064 mmol) were introduced along with TEA (30 μL, 0.41 mmol). The resulting mixture stirred until complete by LCMS at which point the reaction mixture was quenched with water and extracted with DCM (3×). The combined organic extracts were dried over anhydrous Na₂SO_(4(s)), filtered, and concentrated in vacuo. The residue was purified first by C18 reverse phase chromatography (using 20-80% ACN/water as the gradient eluent) then by silica chromatography (using 0-25% MeOH/EtOAc as the gradient eluent) to cleanly afford the title compound (1.3 mg, 4% yield). MS (apci) m/z=519.0 (M+H).

Examples 119 and 120 tert-butyl ((1R,5S,6r)-3-(5-(3-cyano-6-(1-methyl-IH-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)-3-azabicyclo[3.1.1]heptan-6-yl)carbamate (Ex. 119) and 4-(6-((1R,5S,6r)-6-amino-3-azabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile (Ex. 120)

A suspension of 4-(6-fluoropyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile (Intermediate P7; 30 mg, 0.094 mmol), tert-butyl ((1R,5S,6r)-3-azabicyclo[3.1.1]heptan-6-yl)carbamate (24 mg, 0.11 mmol) and Cs₂CO_(3(s)) (153 mg, 0.47 mmol) in DMSO (0.5 mL) was stirred overnight at 90° C. in a sealed pressure vessel. After cooling to ambient temperature, the reaction mixture was poured into 2 N NaOH_((aq)) (2 mL), and extracted in a PS frit with 10% iPrOH in DCM (2×5 mL). The combined organic extracts were concentrated in vacuo and the residue was purified by C18 reverse phase chromatography (using 0-60% ACN/water as the gradient eluent) to afford the title compounds:

Peak 2: Example 119: tert-butyl ((1R,5S,6r)-3-(5-(3-cyano-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl)pyridin-2-yl)-3-azabicyclo[3.1.1]heptan-6-yl)carbamate (15 mg, 31% yield). MS (apci) m/z=512.2 (M+H).

Peak 1: Example 120: 4-(6-((1R,5S,6r)-6-amino-3-azabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile (17 mg, 44% yield). MS (apci) m/z=412.2 (M+H).

Example 121

4-(6-(4-((6-methoxypyridin-3-yl)methyl)piperazin-1-yl)pyridin-3-yl)-6-(3-methyl-1H-pyrazol-5-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile

A mixture of 6-bromo-4-(6-(4-((6-methoxypyridin-3-yl)methyl)piperazin-1-yl)pyridin-3-yl)pyrazolo[1,5-a]pyrazine-3-carbonitrile (Intermediate P9; 58 mg, 0.11 mmol), 3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (0.029 g, 0.14 mmol), 2 M Na₂CO_(3(aq)) (0.13 mL, 0.25 mmol) and Pd(PPh₃)₄ (13 mg, 0.011 mmol) were suspended in 1,4-dioxane (1.1 mL). The resulting mixture was sparged with Ar_((g)) for 15 min, then sealed and stirred overnight at 90° C. After cooling to ambient temperature, the reaction mixture was partitioned between DCM and water, and the combined organic extracts were washed sequentially with water and brine. The combined organic extracts were dried over anhydrous Na₂SO_(4(s)), filtered, and concentrated in vacuo. The crude residue was purified by C18 reverse phase chromatography (using 0-60% ACN/water as the gradient eluent) to afford the TFA salt of the title compound. The TFA salt was suspended in DCM and washed with saturated Na₂CO_(3(s)). The resulting organic extracts were dried over anhydrous Na₂SO_(4(s)), filtered, and concentrated in vacuo to cleanly afford the title compound (17 mg, 29% yield). MS (apci) m/z=507.3 (M+H).

Abbreviations

ACN Acetonitrile Boc-anhydride di-tert-butyl dicarbonate Cu(OAc)₂ Copper diacetate d day, days DCE 1,2-Dichloroethane DCM Dichloromethane DIEA N,N-Diisopropylethylamine DI water Deionized water DMA N,N-Dimethylacetamide DMAP 4-Dimethylaminopyridine DME 1,2-Dimethoxyethane DMF N,N-Dimethylformamide DMSO Dimethylsulfoxide EDC-HCl 1-Ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride Et₂O Diethyl Ether EtOAc Ethyl Acetate EtOH Ethanol eq equivalent h hour, hours HATU 1-[Bis(dimethylamino)methylene]-1H-1,2,3- triazolo[4,5-b]pyridinium 3-oxide hexafluoro- phosphate or 2-(7-Aza-1H-benzotriazole-1-yl)- 1,1,3,3-tetramethyluronium hexafluorophosphate HBTU 3-[Bis(dimethylamino)methyliumyl]-3H-benzo- triazol-1-oxide hexafluorophosphate or 2-(1H- benzotriazole-1-yl)-1,1,3,3-tetramethyluronium hexafluorophosphate HOAc Acetic Acid iPrOH Isopropanol i-PrMgCl Isopropyl magnesium chloride KOAc Potassium Acetate LCMS Liquid chromatography-mass spectrometry MeOH Methanol Me₄N(AcO)₃BH Tetramethylammonium Triacetoxyborohydride min minute, minutes MSH o-(mesitylsulfonyl)hydroxylamine MTBE Methyl tert-Butyl Ether NCS N-Chlorosuccinimide NBS N-Bromosuccinimide NIS N-Iodosuccinimide NaBH(AcO)₃ Sodium Triacetoxyborohydride NH₄OAc Ammonium Acetate Pd(PPh₃)₄ Tetrakis(triphenylphosphine)palladium (0) Pd₂(dba)₃ tris(dibenzylideneacetone)dipalladium (0) PdCl₂(dppf)•CH₂Cl₂ 1,1′-Bis(diphenylphosphino)ferrocene- palladium(II)dichloride dichloromethane complex PPTS Pyridinium p-toluenesulfonate PS frit Biotage ® “Isolute Phase Separators” PS paper Whatman ® silicone treated Phase Separators filter paper PVDF (0.45 μm) disc polyvinylidene difluoride membrane with a 0.45-micron pore size rt Room temperature TEA Triethylamine TFA Trifluoroacetic acid THE tetrahydrofuran Triphosgene (bis(trichloromethyl) carbonate X-phos dicyclohexyl(2′,4′,6′-triisopropyl- [1,1′-biphenyl]-2-yl)phosphine 

What is claimed is:
 1. A compound selected from the group consisting of:

or a pharmaceutically acceptable salt thereof.
 2. A pharmaceutical composition comprising a pharmaceutically acceptable carrier or excipient and a compound of claim 1, or a pharmaceutically acceptable salt thereof.
 3. A method for inhibiting rearranged during transfection kinase activity in a patient in need thereof, wherein the method comprises administering to the patient a therapeutically effective amount of a compound of claim 1, or a pharmaceutically acceptable salt thereof.
 4. The method of claim 3, wherein the patient has cancer.
 5. The method of claim 4, wherein the cancer is a rearranged during transfection-associated cancer.
 6. The method of claim 5, wherein the rearranged during transfection-associated cancer is selected from the group consisting of breast cancer, cervical cancer, colorectal cancer, differentiated thyroid cancer, ganglioneuromatosis of the gastroenteric mucosa, lung cancer, medullary thyroid cancer, multiple endocrine neoplasia type 2A, multiple endocrine neoplasia type 2B, papillary renal cell carcinoma, papillary thyroid cancer, parathyroid hyperplasia, pheochromocytoma, and recurrent thyroid cancer.
 7. The method of claim 6, wherein the rearranged during transfection-associated cancer is medullary thyroid cancer.
 8. The method of claim 6, wherein the lung cancer is small cell lung carcinoma, non-small cell lung cancer, bronchioles lung cell carcinoma, or lung adenocarcinoma.
 9. The method of claim 6, wherein the lung cancer is rearranged during transfection fusion lung cancer.
 10. A method for inhibiting rearranged during transfection kinase activity in a patient in need thereof, wherein the method comprises administering to the patient a therapeutically effective amount of the pharmaceutical composition of claim
 2. 11. The method of claim 10, wherein the patient has cancer.
 12. The method of claim 11, wherein the cancer is a rearranged during transfection-associated cancer.
 13. The method of claim 12, wherein the rearranged during transfection-associated cancer is selected from the group consisting of breast cancer, cervical cancer, colorectal cancer, differentiated thyroid cancer, ganglioneuromatosis of the gastroenteric mucosa, lung cancer, medullary thyroid cancer, multiple endocrine neoplasia type 2A, multiple endocrine neoplasia type 2B, papillary renal cell carcinoma, papillary thyroid cancer, parathyroid hyperplasia, pheochromocytoma, and recurrent thyroid cancer.
 14. The method of claim 13, wherein the rearranged during transfection-associated cancer is medullary thyroid cancer.
 15. The method of claim 13, wherein the lung cancer is small cell lung carcinoma, non-small cell lung cancer, bronchioles lung cell carcinoma, or lung adenocarcinoma.
 16. The method of claim 13, wherein the lung cancer is rearranged during transfection fusion lung cancer. 